Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
14 | g.23416083A>C | CA389037453 | MHRT,MYH7 | c.4874T>G (p.Met1625Arg) n.344A>C | ClinVar |
14 | g.23416083A>G | CA389037455 | MHRT,MYH7 | c.4874T>C (p.Met1625Thr) n.344A>G | gnomAD v4 |
14 | g.23416083A>T | CA389037454 | MHRT,MYH7 | c.4874T>A (p.Met1625Lys) n.344A>T | |
14 | g.23416084T>A | CA389037456 | MHRT,MYH7 | c.4873A>T (p.Met1625Leu) n.345T>A | dbSNP gnomAD v3 gnomAD v4 |
14 | g.23416084T>C | CA389037458 | MHRT,MYH7 | c.4873A>G (p.Met1625Val) n.345T>C | |
14 | g.23416084T>G | CA389037457 | MHRT,MYH7 | c.4873A>C (p.Met1625Leu) n.345T>G | |
14 | g.23416084T= | CA2123465268 | MHRT,MYH7 | c.4873A= (p.Met1625=) n.345T= | |
14 | g.23416085C>A | CA389037459 | MHRT,MYH7 | c.4872G>T (p.Glu1624Asp) n.346C>A | ClinVar dbSNP gnomAD v3 gnomAD v4 |
14 | g.23416085C= | CA2123465272 | MHRT,MYH7 | c.4872G= (p.Glu1624=) n.346C= | |
14 | g.23416085C>G | CA389037460 | MHRT,MYH7 | c.4872G>C (p.Glu1624Asp) n.346C>G | |
14 | g.23416085C>T | CA044101 | MHRT,MYH7 | c.4872G>A (p.Glu1624=) n.346C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.23416086T>A | CA389037461 | MHRT,MYH7 | c.4871A>T (p.Glu1624Val) n.347T>A | |
14 | g.23416086T>C | CA389037462 | MHRT,MYH7 | c.4871A>G (p.Glu1624Gly) n.347T>C | |
14 | g.23416086T>G | CA389037463 | MHRT,MYH7 | c.4871A>C (p.Glu1624Ala) n.347T>G | gnomAD v4 |
14 | g.23416087C>A | CA389037464 | MHRT,MYH7 | c.4870G>T (p.Glu1624Ter) n.348C>A | |
14 | g.23416087C>G | CA389037465 | MHRT,MYH7 | c.4870G>C (p.Glu1624Gln) n.348C>G | COSMIC |
14 | g.23416087C>T | CA389037466 | MHRT,MYH7 | c.4870G>A (p.Glu1624Lys) n.348C>T | ClinVar dbSNP |
14 | g.23416088A= | CA2123465278 | MHRT,MYH7 | c.4869T= (p.Asn1623=) n.349A= | |
14 | g.23416088A>C | CA389037467 | MHRT,MYH7 | c.4869T>G (p.Asn1623Lys) n.349A>C | |
14 | g.23416088A>G | CA485766500 | MHRT,MYH7 | c.4869T>C (p.Asn1623=) n.349A>G | ClinVar dbSNP gnomAD v2 gnomAD v4 |
14 | g.23416088A>T | CA389037468 | MHRT,MYH7 | c.4869T>A (p.Asn1623Lys) n.349A>T | |
14 | g.23416089T>A | CA389037471 | MHRT,MYH7 | c.4868A>T (p.Asn1623Ile) n.350T>A | |
14 | g.23416089T>C | CA389037470 | MHRT,MYH7 | c.4868A>G (p.Asn1623Ser) n.350T>C | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.23416089T>G | CA389037469 | MHRT,MYH7 | c.4868A>C (p.Asn1623Thr) n.350T>G | |
14 | g.23416089T= | CA2123465284 | MHRT,MYH7 | c.4868A= (p.Asn1623=) n.350T= | |
14 | g.23416090T>A | CA389037472 | MHRT,MYH7 | c.4867A>T (p.Asn1623Tyr) n.351T>A | |
14 | g.23416090T>C | CA389037473 | MHRT,MYH7 | c.4867A>G (p.Asn1623Asp) n.351T>C | |
14 | g.23416090T>G | CA389037474 | MHRT,MYH7 | c.4867A>C (p.Asn1623His) n.351T>G | |
14 | g.23416091G>A | CA485766501 | MHRT,MYH7 | c.4866C>T (p.Leu1622=) n.352G>A | ClinVar dbSNP gnomAD v4 |
14 | g.23416091G>C | CA485766502 | MHRT,MYH7 | c.4866C>G (p.Leu1622=) n.352G>C | |
14 | g.23416091G= | CA2123465289 | MHRT,MYH7 | c.4866C= (p.Leu1622=) n.352G= | |
14 | g.23416091G>T | CA485766503 | MHRT,MYH7 | c.4866C>A (p.Leu1622=) n.352G>T | ClinVar dbSNP gnomAD v4 |
14 | g.23416092A>C | CA389037475 | MHRT,MYH7 | c.4865T>G (p.Leu1622Arg) n.353A>C | |
14 | g.23416092A>G | CA389037476 | MHRT,MYH7 | c.4865T>C (p.Leu1622Pro) n.353A>G | |
14 | g.23416092A>T | CA389037477 | MHRT,MYH7 | c.4865T>A (p.Leu1622His) n.353A>T | gnomAD v4 |
14 | g.23416093G>A | CA015424 | MHRT,MYH7 | c.4864C>T (p.Leu1622Phe) n.354G>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.23416093G>C | CA389037478 | MHRT,MYH7 | c.4864C>G (p.Leu1622Val) n.354G>C | |
14 | g.23416093G= | CA2123465295 | MHRT,MYH7 | c.4864C= (p.Leu1622=) n.354G= | |
14 | g.23416093G>T | CA389037479 | MHRT,MYH7 | c.4864C>A (p.Leu1622Ile) n.354G>T | |
14 | g.23416094G>A | CA485766504 | MHRT,MYH7 | c.4863C>T (p.Asp1621=) n.355G>A | ClinVar |
14 | g.23416094G>C | CA389037480 | MHRT,MYH7 | c.4863C>G (p.Asp1621Glu) n.355G>C | |
14 | g.23416094G>T | CA389037481 | MHRT,MYH7 | c.4863C>A (p.Asp1621Glu) n.355G>T | |
14 | g.23416095T>A | CA389037484 | MHRT,MYH7 | c.4862A>T (p.Asp1621Val) n.356T>A | |
14 | g.23416095T>C | CA389037483 | MHRT,MYH7 | c.4862A>G (p.Asp1621Gly) n.356T>C | |
14 | g.23416095T>G | CA389037482 | MHRT,MYH7 | c.4862A>C (p.Asp1621Ala) n.356T>G | dbSNP |
14 | g.23416095T= | CA2123465302 | MHRT,MYH7 | c.4862A= (p.Asp1621=) n.356T= | |
14 | g.23416096C>A | CA389037485 | MHRT,MYH7 | c.4861G>T (p.Asp1621Tyr) n.357C>A | |
14 | g.23416096C= | CA2123465303 | MHRT,MYH7 | c.4861G= (p.Asp1621=) n.357C= | |
14 | g.23416096C>G | CA389037486 | MHRT,MYH7 | c.4861G>C (p.Asp1621His) n.357C>G | |
14 | g.23416096C>T | CA044085 | MHRT,MYH7 | c.4861G>A (p.Asp1621Asn) n.357C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
14 | g.23416097T>A | CA485766505 | MHRT,MYH7 | c.4860A>T (p.Gly1620=) n.358T>A | |
14 | g.23416097T>C | CA485766506 | MHRT,MYH7 | c.4860A>G (p.Gly1620=) n.358T>C | ClinVar dbSNP gnomAD v4 |
14 | g.23416097T>G | CA485766507 | MHRT,MYH7 | c.4860A>C (p.Gly1620=) n.358T>G | dbSNP |
14 | g.23416097T= | CA2123465307 | MHRT,MYH7 | c.4860A= (p.Gly1620=) n.358T= | |
14 | g.23416098C>A | CA389037487 | MHRT,MYH7 | c.4859G>T (p.Gly1620Val) n.359C>A | |
14 | g.23416098C>G | CA389037488 | MHRT,MYH7 | c.4859G>C (p.Gly1620Ala) n.359C>G | |
14 | g.23416098C>T | CA389037489 | MHRT,MYH7 | c.4859G>A (p.Gly1620Glu) n.359C>T | |
14 | g.23416099C>A | CA389037490 | MHRT,MYH7 | c.4858G>T (p.Gly1620Ter) n.360C>A | |
14 | g.23416099C>G | CA389037491 | MHRT,MYH7 | c.4858G>C (p.Gly1620Arg) n.360C>G | |
14 | g.23416099C>T | CA389037492 | MHRT,MYH7 | c.4858G>A (p.Gly1620Arg) n.360C>T | |
14 | g.23416100T>A | CA389037493 | MHRT,MYH7 | c.4857A>T (p.Glu1619Asp) n.361T>A | |
14 | g.23416100T>C | CA485766508 | MHRT,MYH7 | c.4857A>G (p.Glu1619=) n.361T>C | ClinVar dbSNP |
14 | g.23416100T>G | CA389037494 | MHRT,MYH7 | c.4857A>C (p.Glu1619Asp) n.361T>G | |
14 | g.23416100T= | CA2123465310 | MHRT,MYH7 | c.4857A= (p.Glu1619=) n.361T= | |
14 | g.23416101T>A | CA389037497 | MHRT,MYH7 | c.4856A>T (p.Glu1619Val) n.362T>A | |
14 | g.23416101T>C | CA389037496 | MHRT,MYH7 | c.4856A>G (p.Glu1619Gly) n.362T>C | |
14 | g.23416101T>G | CA389037495 | MHRT,MYH7 | c.4856A>C (p.Glu1619Ala) n.362T>G | |
14 | g.23416113_23416114insACTTCAGTCTGGAGCTGGGACAGGTCAGCATCCATCTTCTTCT | CA044072 | MHRT,MYH7 | c.4856_4857insTGCTGACCTGTCCCAGCTCCAGACTGAAGTAGAAGAAGATGGA (p.Glu1619AspfsTer20) n.374_375insACTTCAGTCTGGAGCTGGGACAGGTCAGCATCCATCTTCTTCT | dbSNP ExAC |
14 | g.23416102C>A | CA389037498 | MHRT,MYH7 | c.4855G>T (p.Glu1619Ter) n.363C>A | |
14 | g.23416102C= | CA2123465321 | MHRT,MYH7 | c.4855G= (p.Glu1619=) n.363C= | |
14 | g.23416102C>G | CA389037499 | MHRT,MYH7 | c.4855G>C (p.Glu1619Gln) n.363C>G | |
14 | g.23416102C>T | CA015416 | MHRT,MYH7 | c.4855G>A (p.Glu1619Lys) n.363C>T | ClinVar dbSNP |
14 | g.23416103C>A | CA389037500 | MHRT,MYH7 | c.4854G>T (p.Met1618Ile) n.364C>A | |
14 | g.23416103C>G | CA389037501 | MHRT,MYH7 | c.4854G>C (p.Met1618Ile) n.364C>G | |
14 | g.23416103C>T | CA389037502 | MHRT,MYH7 | c.4854G>A (p.Met1618Ile) n.364C>T | |
14 | g.23416104A= | CA2123465328 | MHRT,MYH7 | c.4853T= (p.Met1618=) n.365A= | |
14 | g.23416104A>C | CA389037503 | MHRT,MYH7 | c.4853T>G (p.Met1618Arg) n.365A>C | |
14 | g.23416104A>G | CA389037504 | MHRT,MYH7 | c.4853T>C (p.Met1618Thr) n.365A>G | ClinVar dbSNP gnomAD v2 gnomAD v4 |
14 | g.23416104A>T | CA389037505 | MHRT,MYH7 | c.4853T>A (p.Met1618Lys) n.365A>T | |
14 | g.23416104_23416107delinsATCT | CA2123465326 | MHRT,MYH7 | c.4850_4853delinsAGAT (p.Lys1617=) n.365_368delinsATCT | |
14 | g.23416105T>A | CA389037506 | MHRT,MYH7 | c.4852A>T (p.Met1618Leu) n.366T>A | |
14 | g.23416105T>C | CA389037507 | MHRT,MYH7 | c.4852A>G (p.Met1618Val) n.366T>C | |
14 | g.23416105T>G | CA389037508 | MHRT,MYH7 | c.4852A>C (p.Met1618Leu) n.366T>G | |
14 | g.23416113_23416115dup | CA2580616566 | MHRT,MYH7 | c.4850_4852dup (p.Lys1617_Met1618insLys) n.374_376dup | ClinVar |
14 | g.23416113_23416115del | CA015411 | MHRT,MYH7 | c.4850_4852del (p.Lys1617del) n.374_376del | ClinVar dbSNP |
14 | g.23416106C>A | CA389037510 | MHRT,MYH7 | c.4851G>T (p.Lys1617Asn) n.367C>A | |
14 | g.23416106C>G | CA389037509 | MHRT,MYH7 | c.4851G>C (p.Lys1617Asn) n.367C>G | |
14 | g.23416106C>T | CA485766509 | MHRT,MYH7 | c.4851G>A (p.Lys1617=) n.367C>T | |
14 | g.23416107T>A | CA389037511 | MHRT,MYH7 | c.4850A>T (p.Lys1617Met) n.368T>A | |
14 | g.23416107T>C | CA389037513 | MHRT,MYH7 | c.4850A>G (p.Lys1617Arg) n.368T>C | |
14 | g.23416107T>G | CA389037512 | MHRT,MYH7 | c.4850A>C (p.Lys1617Thr) n.368T>G | |
14 | g.23416108T>A | CA389037514 | MHRT,MYH7 | c.4849A>T (p.Lys1617Ter) n.369T>A | |
14 | g.23416108T>C | CA389037516 | MHRT,MYH7 | c.4849A>G (p.Lys1617Glu) n.369T>C | |
14 | g.23416108T>G | CA389037515 | MHRT,MYH7 | c.4849A>C (p.Lys1617Gln) n.369T>G | |
14 | g.23416109C>A | CA389037517 | MHRT,MYH7 | c.4848G>T (p.Lys1616Asn) n.370C>A | |
14 | g.23416109C= | CA2123465341 | MHRT,MYH7 | c.4848G= (p.Lys1616=) n.370C= | |
14 | g.23416109C>G | CA389037518 | MHRT,MYH7 | c.4848G>C (p.Lys1616Asn) n.370C>G | |
14 | g.23416109C>T | CA044065 | MHRT,MYH7 | c.4848G>A (p.Lys1616=) n.370C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
14 | g.23416110T>A | CA389037519 | MHRT,MYH7 | c.4847A>T (p.Lys1616Met) n.371T>A | |
14 | g.23416110T>C | CA389037521 | MHRT,MYH7 | c.4847A>G (p.Lys1616Arg) n.371T>C | dbSNP |
14 | g.23416110T>G | CA389037520 | MHRT,MYH7 | c.4847A>C (p.Lys1616Thr) n.371T>G | |
14 | g.23416110T= | CA2123465344 | MHRT,MYH7 | c.4847A= (p.Lys1616=) n.371T= | |
14 | g.23416111T>A | CA389037522 | MHRT,MYH7 | c.4846A>T (p.Lys1616Ter) n.372T>A | |
14 | g.23416111T>C | CA389037524 | MHRT,MYH7 | c.4846A>G (p.Lys1616Glu) n.372T>C | ClinVar |
14 | g.23416111T>G | CA389037523 | MHRT,MYH7 | c.4846A>C (p.Lys1616Gln) n.372T>G | |
14 | g.23416112C>A | CA16614393 | MHRT,MYH7 | c.4845G>T (p.Lys1615Asn) n.373C>A | ClinVar dbSNP |
14 | g.23416112C= | CA2123465348 | MHRT,MYH7 | c.4845G= (p.Lys1615=) n.373C= | |
14 | g.23416112C>G | CA389037525 | MHRT,MYH7 | c.4845G>C (p.Lys1615Asn) n.373C>G | |
14 | g.23416112C>T | CA485766510 | MHRT,MYH7 | c.4845G>A (p.Lys1615=) n.373C>T | ClinVar dbSNP |
14 | g.23416113T>A | CA389037526 | MHRT,MYH7 | c.4844A>T (p.Lys1615Met) n.374T>A | |
14 | g.23416113T>C | CA389037527 | MHRT,MYH7 | c.4844A>G (p.Lys1615Arg) n.374T>C | |
14 | g.23416113T>G | CA389037528 | MHRT,MYH7 | c.4844A>C (p.Lys1615Thr) n.374T>G | |
14 | g.23416114T>A | CA389037531 | MHRT,MYH7 | c.4843A>T (p.Lys1615Ter) n.375T>A | |
14 | g.23416114T>C | CA389037530 | MHRT,MYH7 | c.4843A>G (p.Lys1615Glu) n.375T>C | |
14 | g.23416114T>G | CA389037529 | MHRT,MYH7 | c.4843A>C (p.Lys1615Gln) n.375T>G | |
14 | g.23416115C>A | CA485766511 | MHRT,MYH7 | c.4842G>T (p.Val1614=) n.376C>A | |
14 | g.23416115C>G | CA485766512 | MHRT,MYH7 | c.4842G>C (p.Val1614=) n.376C>G | |
14 | g.23416115C>T | CA485766513 | MHRT,MYH7 | c.4842G>A (p.Val1614=) n.376C>T | |
14 | g.23416116A= | CA2123465352 | MHRT,MYH7 | c.4841T= (p.Val1614=) n.377A= | |
14 | g.23416116A>C | CA389037532 | MHRT,MYH7 | c.4841T>G (p.Val1614Gly) n.377A>C | dbSNP |
14 | g.23416116A>G | CA389037533 | MHRT,MYH7 | c.4841T>C (p.Val1614Ala) n.377A>G | |
14 | g.23416116A>T | CA389037534 | MHRT,MYH7 | c.4841T>A (p.Val1614Glu) n.377A>T | |
14 | g.23416117C>A | CA389037535 | MHRT,MYH7 | c.4840G>T (p.Val1614Leu) n.378C>A | dbSNP gnomAD v2 gnomAD v4 |
14 | g.23416117C= | CA2123465356 | MHRT,MYH7 | c.4840G= (p.Val1614=) n.378C= | |
14 | g.23416117C>G | CA389037536 | MHRT,MYH7 | c.4840G>C (p.Val1614Leu) n.378C>G | |
14 | g.23416117C>T | CA389037537 | MHRT,MYH7 | c.4840G>A (p.Val1614Met) n.378C>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.23416118C>A | CA389037538 | MHRT,MYH7 | c.4839G>T (p.Arg1613Ser) n.379C>A | |
14 | g.23416118C= | CA2123465361 | MHRT,MYH7 | c.4839G= (p.Arg1613=) n.379C= | |
14 | g.23416118C>G | CA389037539 | MHRT,MYH7 | c.4839G>C (p.Arg1613Ser) n.379C>G | |
14 | g.23416118C>T | CA044050 | MHRT,MYH7 | c.4839G>A (p.Arg1613=) n.379C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
14 | g.23416119C>A | CA389037540 | MHRT,MYH7 | c.4838G>T (p.Arg1613Met) n.380C>A | |
14 | g.23416119C= | CA2123465366 | MHRT,MYH7 | c.4838G= (p.Arg1613=) n.380C= | |
14 | g.23416119C>G | CA389037541 | MHRT,MYH7 | c.4838G>C (p.Arg1613Thr) n.380C>G | gnomAD v4 |
14 | g.23416119C>T | CA015403 | MHRT,MYH7 | c.4838G>A (p.Arg1613Lys) n.380C>T | ClinVar dbSNP |
14 | g.23416120T>A | CA389037542 | MHRT,MYH7 | c.4837A>T (p.Arg1613Trp) n.381T>A | |
14 | g.23416120T>C | CA389037543 | MHRT,MYH7 | c.4837A>G (p.Arg1613Gly) n.381T>C | |
14 | g.23416120T>G | CA485766514 | MHRT,MYH7 | c.4837A>C (p.Arg1613=) n.381T>G | ClinVar dbSNP |
14 | g.23416120T= | CA2123465375 | MHRT,MYH7 | c.4837A= (p.Arg1613=) n.381T= | |
14 | g.23416121C>A | CA485766515 | MHRT,MYH7 | c.4836G>T (p.Leu1612=) n.382C>A | |
14 | g.23416121C= | CA2123465383 | MHRT,MYH7 | c.4836G= (p.Leu1612=) n.382C= | |
14 | g.23416121C>G | CA485766516 | MHRT,MYH7 | c.4836G>C (p.Leu1612=) n.382C>G | gnomAD v4 |
14 | g.23416121C>T | CA485766517 | MHRT,MYH7 | c.4836G>A (p.Leu1612=) n.382C>T | dbSNP |
14 | g.23416122A= | CA2123465389 | MHRT,MYH7 | c.4835T= (p.Leu1612=) n.383A= | |
14 | g.23416122A>C | CA389037544 | MHRT,MYH7 | c.4835T>G (p.Leu1612Arg) n.383A>C | |
14 | g.23416122A>G | CA015395 | MHRT,MYH7 | c.4835T>C (p.Leu1612Pro) n.383A>G | ClinVar dbSNP |
14 | g.23416122A>T | CA389037545 | MHRT,MYH7 | c.4835T>A (p.Leu1612Gln) n.383A>T | |
14 | g.23416123G>A | CA044032 | MHRT,MYH7 | c.4834C>T (p.Leu1612=) n.384G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
14 | g.23416123G>C | CA015389 | MHRT,MYH7 | c.4834C>G (p.Leu1612Val) n.384G>C | ClinVar dbSNP |
14 | g.23416123G= | CA2123465403 | MHRT,MYH7 | c.4834C= (p.Leu1612=) n.384G= | |
14 | g.23416123G>T | CA389037546 | MHRT,MYH7 | c.4834C>A (p.Leu1612Met) n.384G>T | |
14 | g.23416124G>A | CA485766518 | MHRT,MYH7 | c.4833C>T (p.Ala1611=) n.385G>A | gnomAD v4 |
14 | g.23416124G>C | CA485766519 | MHRT,MYH7 | c.4833C>G (p.Ala1611=) n.385G>C | |
14 | g.23416124G>T | CA485766520 | MHRT,MYH7 | c.4833C>A (p.Ala1611=) n.385G>T | |
14 | g.23416125G>A | CA044022 | MHRT,MYH7 | c.4832C>T (p.Ala1611Val) n.386G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
14 | g.23416125G>C | CA389037548 | MHRT,MYH7 | c.4832C>G (p.Ala1611Gly) n.386G>C | |
14 | g.23416125G= | CA2123465413 | MHRT,MYH7 | c.4832C= (p.Ala1611=) n.386G= | |
14 | g.23416125G>T | CA389037547 | MHRT,MYH7 | c.4832C>A (p.Ala1611Asp) n.386G>T | |
14 | g.23416126C>A | CA015382 | MHRT,MYH7 | c.4831G>T (p.Ala1611Ser) n.387C>A | ClinVar dbSNP ExAC gnomAD v3 gnomAD v4 |
14 | g.23416126C= | CA2123465419 | MHRT,MYH7 | c.4831G= (p.Ala1611=) n.387C= | |
14 | g.23416126C>G | CA389037549 | MHRT,MYH7 | c.4831G>C (p.Ala1611Pro) n.387C>G | |
14 | g.23416126C>T | CA389037550 | MHRT,MYH7 | c.4831G>A (p.Ala1611Thr) n.387C>T | ClinVar |
14 | g.23416127C>A | CA389037551 | MHRT,MYH7 | c.4830G>T (p.Glu1610Asp) n.388C>A | |
14 | g.23416127C>G | CA389037552 | MHRT,MYH7 | c.4830G>C (p.Glu1610Asp) n.388C>G | |
14 | g.23416127C>T | CA485766521 | MHRT,MYH7 | c.4830G>A (p.Glu1610=) n.388C>T | |
14 | g.23416128T>A | CA389037553 | MHRT,MYH7 | c.4829A>T (p.Glu1610Val) n.389T>A | |
14 | g.23416128T>C | CA389037554 | MHRT,MYH7 | c.4829A>G (p.Glu1610Gly) n.389T>C | |
14 | g.23416128T>G | CA389037555 | MHRT,MYH7 | c.4829A>C (p.Glu1610Ala) n.389T>G | |
14 | g.23416128_23416131delinsTCGT | CA2123465429 | MHRT,MYH7 | c.4826_4829delinsACGA (p.Asn1609=) n.389_392delinsTCGT | |
14 | g.23416129C>A | CA389037556 | MHRT,MYH7 | c.4828G>T (p.Glu1610Ter) n.390C>A | |
14 | g.23416129C= | CA2123465441 | MHRT,MYH7 | c.4828G= (p.Glu1610=) n.390C= | |
14 | g.23416129C>G | CA015373 | MHRT,MYH7 | c.4828G>C (p.Glu1610Gln) n.390C>G | ClinVar dbSNP gnomAD v4 |
14 | g.23416129C>T | CA10645050 | MHRT,MYH7 | c.4828G>A (p.Glu1610Lys) n.390C>T | ClinVar dbSNP gnomAD v4 |
14 | g.23416129_23416131delinsGGTTGCGGC | CA658658243 | MHRT,MYH7 | c.4826_4828delinsGCCGCAACC (p.Asn1609_Glu1610delinsSerArgAsnGln) n.390_392delinsGGTTGCGGC | ClinVar dbSNP |
14 | g.23416130G>A | CA015366 | MHRT,MYH7 | c.4827C>T (p.Asn1609=) n.391G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
14 | g.23416130G>C | CA389037558 | MHRT,MYH7 | c.4827C>G (p.Asn1609Lys) n.391G>C | dbSNP gnomAD v2 gnomAD v4 |
14 | g.23416130G= | CA2123465452 | MHRT,MYH7 | c.4827C= (p.Asn1609=) n.391G= | |
14 | g.23416130G>T | CA389037557 | MHRT,MYH7 | c.4827C>A (p.Asn1609Lys) n.391G>T | gnomAD v4 |
14 | g.23416131T>A | CA389037559 | MHRT,MYH7 | c.4826A>T (p.Asn1609Ile) n.392T>A | |
14 | g.23416131T>C | CA389037560 | MHRT,MYH7 | c.4826A>G (p.Asn1609Ser) n.392T>C | |
14 | g.23416131T>G | CA389037561 | MHRT,MYH7 | c.4826A>C (p.Asn1609Thr) n.392T>G | |
14 | g.23416132T>A | CA389037562 | MHRT,MYH7 | c.4825A>T (p.Asn1609Tyr) n.393T>A | |
14 | g.23416132T>C | CA389037563 | MHRT,MYH7 | c.4825A>G (p.Asn1609Asp) n.393T>C | |
14 | g.23416132T>G | CA389037564 | MHRT,MYH7 | c.4825A>C (p.Asn1609His) n.393T>G | dbSNP gnomAD v2 gnomAD v4 |
14 | g.23416132T= | CA2123465459 | MHRT,MYH7 | c.4825A= (p.Asn1609=) n.393T= | |
14 | g.23416133G>A | CA485766522 | MHRT,MYH7 | c.4824C>T (p.Arg1608=) n.394G>A | |
14 | g.23416133G>C | CA485766523 | MHRT,MYH7 | c.4824C>G (p.Arg1608=) n.394G>C | |
14 | g.23416133G>T | CA485766524 | MHRT,MYH7 | c.4824C>A (p.Arg1608=) n.394G>T | |
14 | g.23416134C>A | CA043989 | MHRT,MYH7 | c.4823G>T (p.Arg1608Leu) n.395C>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
14 | g.23416134C= | CA2123465468 | MHRT,MYH7 | c.4823G= (p.Arg1608=) n.395C= | |
14 | g.23416134C>G | CA015359 | MHRT,MYH7 | c.4823G>C (p.Arg1608Pro) n.395C>G | ClinVar dbSNP |
14 | g.23416134C>T | CA043977 | MHRT,MYH7 | c.4823G>A (p.Arg1608His) n.395C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
14 | g.23416135G>A | CA043961 | MHRT,MYH7 | c.4822C>T (p.Arg1608Cys) n.396G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
14 | g.23416135G>C | CA389037565 | MHRT,MYH7 | c.4822C>G (p.Arg1608Gly) n.396G>C | |
14 | g.23416135G= | CA2123465475 | MHRT,MYH7 | c.4822C= (p.Arg1608=) n.396G= | |
14 | g.23416135G>T | CA389037566 | MHRT,MYH7 | c.4822C>A (p.Arg1608Ser) n.396G>T | |
14 | g.23416136G>A | CA485766525 | MHRT,MYH7 | c.4821C>T (p.Ser1607=) n.397G>A | COSMIC |
14 | g.23416136G>C | CA389037567 | MHRT,MYH7 | c.4821C>G (p.Ser1607Arg) n.397G>C | gnomAD v4 |
14 | g.23416136G= | CA2123465483 | MHRT,MYH7 | c.4821C= (p.Ser1607=) n.397G= | |
14 | g.23416136G>T | CA043942 | MHRT,MYH7 | c.4821C>A (p.Ser1607Arg) n.397G>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
14 | g.23416137C>A | CA389037568 | MHRT,MYH7 | c.4820G>T (p.Ser1607Ile) n.398C>A | |
14 | g.23416137C= | CA2123465485 | MHRT,MYH7 | c.4820G= (p.Ser1607=) n.398C= | |
14 | g.23416137C>G | CA257810583 | MHRT,MYH7 | c.4820G>C (p.Ser1607Thr) n.398C>G | dbSNP |
14 | g.23416137C>T | CA389037569 | MHRT,MYH7 | c.4820G>A (p.Ser1607Asn) n.398C>T | ClinVar |
14 | g.23416138T>A | CA389037570 | MHRT,MYH7 | c.4819A>T (p.Ser1607Cys) n.399T>A | |
14 | g.23416138T>C | CA389037571 | MHRT,MYH7 | c.4819A>G (p.Ser1607Gly) n.399T>C | ClinVar dbSNP |
14 | g.23416138T>G | CA389037572 | MHRT,MYH7 | c.4819A>C (p.Ser1607Arg) n.399T>G | |
14 | g.23416138T= | CA2123465487 | MHRT,MYH7 | c.4819A= (p.Ser1607=) n.399T= | |
14 | g.23416139G>A | CA485766526 | MHRT,MYH7 | c.4818C>T (p.Arg1606=) n.400G>A | |
14 | g.23416139G>C | CA485766527 | MHRT,MYH7 | c.4818C>G (p.Arg1606=) n.400G>C | |
14 | g.23416139G= | CA2123465490 | MHRT,MYH7 | c.4818C= (p.Arg1606=) n.400G= | |
14 | g.23416139G>T | CA043912 | MHRT,MYH7 | c.4818C>A (p.Arg1606=) n.400G>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.23416140C>A | CA389037573 | MHRT,MYH7 | c.4817G>T (p.Arg1606Leu) n.401C>A | |
14 | g.23416140C= | CA2123465495 | MHRT,MYH7 | c.4817G= (p.Arg1606=) n.401C= | |
14 | g.23416140C>G | CA389037574 | MHRT,MYH7 | c.4817G>C (p.Arg1606Pro) n.401C>G | ClinVar dbSNP |
14 | g.23416140C>T | CA015352 | MHRT,MYH7 | c.4817G>A (p.Arg1606His) n.401C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
14 | g.23416140_23416142delinsCGT | CA2123465501 | MHRT,MYH7 | c.4815_4817delinsACG (p.Thr1605=) n.401_403delinsCGT | |
14 | g.23416141G>A | CA015344 | MHRT,MYH7 | c.4816C>T (p.Arg1606Cys) n.402G>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.23416141G>C | CA389037575 | MHRT,MYH7 | c.4816C>G (p.Arg1606Gly) n.402G>C | ClinVar gnomAD v4 |
14 | g.23416141G= | CA2123465525 | MHRT,MYH7 | c.4816C= (p.Arg1606=) n.402G= | |
14 | g.23416141G>T | CA389037576 | MHRT,MYH7 | c.4816C>A (p.Arg1606Ser) n.402G>T | |
14 | g.23416143_23416144del | CA2123465517 | MHRT,MYH7 | c.4815_4816del (p.Arg1606GlnfsTer18) n.404_405del | ClinVar dbSNP gnomAD v4 |
14 | g.23416142T>A | CA485766528 | MHRT,MYH7 | c.4815A>T (p.Thr1605=) n.403T>A | ClinVar dbSNP gnomAD v4 |
14 | g.23416142T>C | CA043888 | MHRT,MYH7 | c.4815A>G (p.Thr1605=) n.403T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.23416142T>G | CA485766529 | MHRT,MYH7 | c.4815A>C (p.Thr1605=) n.403T>G | |
14 | g.23416142T= | CA2123465532 | MHRT,MYH7 | c.4815A= (p.Thr1605=) n.403T= | |
14 | g.23416143G>A | CA389037579 | MHRT,MYH7 | c.4814C>T (p.Thr1605Ile) n.404G>A | dbSNP gnomAD v3 gnomAD v4 |
14 | g.23416143G>C | CA389037578 | MHRT,MYH7 | c.4814C>G (p.Thr1605Arg) n.404G>C | dbSNP |
14 | g.23416143G= | CA2123465539 | MHRT,MYH7 | c.4814C= (p.Thr1605=) n.404G= | |
14 | g.23416143G>T | CA389037577 | MHRT,MYH7 | c.4814C>A (p.Thr1605Lys) n.404G>T | |
14 | g.23416144T>A | CA389037580 | MHRT,MYH7 | c.4813A>T (p.Thr1605Ser) n.405T>A | dbSNP |
14 | g.23416144T>C | CA389037581 | MHRT,MYH7 | c.4813A>G (p.Thr1605Ala) n.405T>C | |
14 | g.23416144T>G | CA389037582 | MHRT,MYH7 | c.4813A>C (p.Thr1605Pro) n.405T>G | |
14 | g.23416144T= | CA2123465542 | MHRT,MYH7 | c.4813A= (p.Thr1605=) n.405T= | |
14 | g.23416147_23416148del | CA2624234337 | MHRT,MYH7 | c.4812_4813del (p.Glu1604AspfsTer20) n.408_409del | gnomAD v4 |
14 | g.23416145C>A | CA389037583 | MHRT,MYH7 | c.4812G>T (p.Glu1604Asp) n.406C>A | |
14 | g.23416145C>G | CA389037584 | MHRT,MYH7 | c.4812G>C (p.Glu1604Asp) n.406C>G | |
14 | g.23416145C>T | CA485766530 | MHRT,MYH7 | c.4812G>A (p.Glu1604=) n.406C>T | |
14 | g.23416146T>A | CA389037585 | MHRT,MYH7 | c.4811A>T (p.Glu1604Val) n.407T>A | |
14 | g.23416146T>C | CA389037586 | MHRT,MYH7 | c.4811A>G (p.Glu1604Gly) n.407T>C | |
14 | g.23416146T>G | CA389037587 | MHRT,MYH7 | c.4811A>C (p.Glu1604Ala) n.407T>G | |
14 | g.23416147C>A | CA389037588 | MHRT,MYH7 | c.4810G>T (p.Glu1604Ter) n.408C>A | |
14 | g.23416147C>G | CA389037589 | MHRT,MYH7 | c.4810G>C (p.Glu1604Gln) n.408C>G | |
14 | g.23416147C>T | CA389037590 | MHRT,MYH7 | c.4810G>A (p.Glu1604Lys) n.408C>T | |
14 | g.23416148T>A | CA485766531 | MHRT,MYH7 | c.4809A>T (p.Ala1603=) n.409T>A | |
14 | g.23416148T>C | CA485766532 | MHRT,MYH7 | c.4809A>G (p.Ala1603=) n.409T>C | ClinVar dbSNP |
14 | g.23416148T>G | CA485766533 | MHRT,MYH7 | c.4809A>C (p.Ala1603=) n.409T>G | dbSNP |
14 | g.23416148T= | CA2123465546 | MHRT,MYH7 | c.4809A= (p.Ala1603=) n.409T= | |
14 | g.23416149G>A | CA389037593 | MHRT,MYH7 | c.4808C>T (p.Ala1603Val) n.410G>A | ClinVar dbSNP |
14 | g.23416149G>C | CA389037592 | MHRT,MYH7 | c.4808C>G (p.Ala1603Gly) n.410G>C | |
14 | g.23416149G= | CA2123465550 | MHRT,MYH7 | c.4808C= (p.Ala1603=) n.410G= | |
14 | g.23416149G>T | CA389037591 | MHRT,MYH7 | c.4808C>A (p.Ala1603Glu) n.410G>T | |
14 | g.23416150C>A | CA389037594 | MHRT,MYH7 | c.4807G>T (p.Ala1603Ser) n.411C>A | gnomAD v4 |
14 | g.23416150C= | CA2123465555 | MHRT,MYH7 | c.4807G= (p.Ala1603=) n.411C= | |
14 | g.23416150C>G | CA347265 | MHRT,MYH7 | c.4807G>C (p.Ala1603Pro) n.411C>G | ClinVar dbSNP |
14 | g.23416150C>T | CA015331 | MHRT,MYH7 | c.4807G>A (p.Ala1603Thr) n.411C>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.23416150_23416154del | CA2800863124 | MHRT,MYH7 | c.4803_4807del (p.Asp1602ArgfsTer21) n.411_415del | |
14 | g.23416151G>A | CA015322 | MHRT,MYH7 | c.4806C>T (p.Asp1602=) n.412G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.23416151G>C | CA389037595 | MHRT,MYH7 | c.4806C>G (p.Asp1602Glu) n.412G>C | |
14 | g.23416151G= | CA2123465568 | MHRT,MYH7 | c.4806C= (p.Asp1602=) n.412G= | |
14 | g.23416151G>T | CA389037596 | MHRT,MYH7 | c.4806C>A (p.Asp1602Glu) n.412G>T | ClinVar gnomAD v4 |
14 | g.23416152T>A | CA389037597 | MHRT,MYH7 | c.4805A>T (p.Asp1602Val) n.413T>A | |
14 | g.23416152T>C | CA389037598 | MHRT,MYH7 | c.4805A>G (p.Asp1602Gly) n.413T>C | |
14 | g.23416152T>G | CA389037599 | MHRT,MYH7 | c.4805A>C (p.Asp1602Ala) n.413T>G | |
14 | g.23416153C>A | CA389037600 | MHRT,MYH7 | c.4804G>T (p.Asp1602Tyr) n.414C>A | |
14 | g.23416153C>G | CA389037601 | MHRT,MYH7 | c.4804G>C (p.Asp1602His) n.414C>G | |
14 | g.23416153C>T | CA389037602 | MHRT,MYH7 | c.4804G>A (p.Asp1602Asn) n.414C>T | |
14 | g.23416154C>A | CA485766534 | MHRT,MYH7 | c.4803G>T (p.Leu1601=) n.415C>A | |
14 | g.23416154C= | CA2123465574 | MHRT,MYH7 | c.4803G= (p.Leu1601=) n.415C= | |
14 | g.23416154C>G | CA485766535 | MHRT,MYH7 | c.4803G>C (p.Leu1601=) n.415C>G | |
14 | g.23416154C>T | CA015317 | MHRT,MYH7 | c.4803G>A (p.Leu1601=) n.415C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.23416155A>C | CA389037605 | MHRT,MYH7 | c.4802T>G (p.Leu1601Arg) n.416A>C | |
14 | g.23416155A>G | CA389037603 | MHRT,MYH7 | c.4802T>C (p.Leu1601Pro) n.416A>G | ClinVar dbSNP |
14 | g.23416155A>T | CA389037604 | MHRT,MYH7 | c.4802T>A (p.Leu1601Gln) n.416A>T | |
14 | g.23416156G>A | CA485766536 | MHRT,MYH7 | c.4801C>T (p.Leu1601=) n.417G>A | |
14 | g.23416156G>C | CA389037606 | MHRT,MYH7 | c.4801C>G (p.Leu1601Val) n.417G>C | ClinVar |
14 | g.23416156G>T | CA389037607 | MHRT,MYH7 | c.4801C>A (p.Leu1601Met) n.417G>T | |
14 | g.23416158del | CA2624234372 | MHRT,MYH7 | c.4801del (p.Leu1601TrpfsTer12) n.419del | gnomAD v4 |
14 | g.23416157G>A | CA16606527 | MHRT,MYH7 | c.4800C>T (p.Ser1600=) n.418G>A | ClinVar dbSNP gnomAD v4 |
14 | g.23416157G>C | CA485766537 | MHRT,MYH7 | c.4800C>G (p.Ser1600=) n.418G>C | |
14 | g.23416157G= | CA2123465585 | MHRT,MYH7 | c.4800C= (p.Ser1600=) n.418G= | |
14 | g.23416157G>T | CA485766538 | MHRT,MYH7 | c.4800C>A (p.Ser1600=) n.418G>T | |
14 | g.23416158G>A | CA389037608 | MHRT,MYH7 | c.4799C>T (p.Ser1600Phe) n.419G>A | ClinVar |
14 | g.23416158G>C | CA389037609 | MHRT,MYH7 | c.4799C>G (p.Ser1600Cys) n.419G>C | |
14 | g.23416158G>T | CA389037610 | MHRT,MYH7 | c.4799C>A (p.Ser1600Tyr) n.419G>T | |
14 | g.23416158_23416159delinsGA | CA2123465590 | MHRT,MYH7 | c.4798_4799delinsTC (p.Ser1600=) n.419_420delinsGA | |
14 | g.23416159del | CA961068778 | MHRT,MYH7 | c.4798del (p.Ser1600ProfsTer13) n.420del | dbSNP gnomAD v3 gnomAD v4 |
14 | g.23416159A>C | CA389037611 | MHRT,MYH7 | c.4798T>G (p.Ser1600Ala) n.420A>C | |
14 | g.23416159A>G | CA389037612 | MHRT,MYH7 | c.4798T>C (p.Ser1600Pro) n.420A>G | ClinVar |
14 | g.23416159A>T | CA389037613 | MHRT,MYH7 | c.4798T>A (p.Ser1600Thr) n.420A>T | |
14 | g.23416160G>A | CA257810607 | MHRT,MYH7 | c.4797C>T (p.Thr1599=) n.421G>A | dbSNP gnomAD v4 |
14 | g.23416160G>C | CA485766539 | MHRT,MYH7 | c.4797C>G (p.Thr1599=) n.421G>C | |
14 | g.23416160G= | CA2123465594 | MHRT,MYH7 | c.4797C= (p.Thr1599=) n.421G= | |
14 | g.23416160G>T | CA485766540 | MHRT,MYH7 | c.4797C>A (p.Thr1599=) n.421G>T | |
14 | g.23416161G>A | CA389037614 | MHRT,MYH7 | c.4796C>T (p.Thr1599Ile) n.422G>A | |
14 | g.23416161G>C | CA389037615 | MHRT,MYH7 | c.4796C>G (p.Thr1599Ser) n.422G>C | |
14 | g.23416161G>T | CA389037616 | MHRT,MYH7 | c.4796C>A (p.Thr1599Asn) n.422G>T | |
14 | g.23416162T>A | CA389037618 | MHRT,MYH7 | c.4795A>T (p.Thr1599Ser) n.423T>A | gnomAD v4 |
14 | g.23416162T>C | CA389037617 | MHRT,MYH7 | c.4795A>G (p.Thr1599Ala) n.423T>C | |
14 | g.23416162T>G | CA015308 | MHRT,MYH7 | c.4795A>C (p.Thr1599Pro) n.423T>G | ClinVar dbSNP |
14 | g.23416162T= | CA2123465601 | MHRT,MYH7 | c.4795A= (p.Thr1599=) n.423T= | |
14 | g.23416163C>A | CA389037619 | MHRT,MYH7 | c.4794G>T (p.Gln1598His) n.424C>A | |
14 | g.23416163C>G | CA389037620 | MHRT,MYH7 | c.4794G>C (p.Gln1598His) n.424C>G | |
14 | g.23416163C>T | CA485766541 | MHRT,MYH7 | c.4794G>A (p.Gln1598=) n.424C>T | |
14 | g.23416164T>A | CA389037621 | MHRT,MYH7 | c.4793A>T (p.Gln1598Leu) n.425T>A | |
14 | g.23416164T>C | CA389037622 | MHRT,MYH7 | c.4793A>G (p.Gln1598Arg) n.425T>C | |
14 | g.23416164T>G | CA389037623 | MHRT,MYH7 | c.4793A>C (p.Gln1598Pro) n.425T>G | ClinVar dbSNP |
14 | g.23416165G>A | CA389037624 | MHRT,MYH7 | c.4792C>T (p.Gln1598Ter) n.426G>A | |
14 | g.23416165G>C | CA389037625 | MHRT,MYH7 | c.4792C>G (p.Gln1598Glu) n.426G>C | |
14 | g.23416165G>T | CA389037626 | MHRT,MYH7 | c.4792C>A (p.Gln1598Lys) n.426G>T | |
14 | g.23416166C>A | CA485766542 | MHRT,MYH7 | c.4791G>T (p.Leu1597=) n.427C>A | |
14 | g.23416166C>G | CA485766543 | MHRT,MYH7 | c.4791G>C (p.Leu1597=) n.427C>G | |
14 | g.23416166C>T | CA485766544 | MHRT,MYH7 | c.4791G>A (p.Leu1597=) n.427C>T | |
14 | g.23416167A>C | CA389037627 | MHRT,MYH7 | c.4790T>G (p.Leu1597Arg) n.428A>C | |
14 | g.23416167A>G | CA389037628 | MHRT,MYH7 | c.4790T>C (p.Leu1597Pro) n.428A>G | ClinVar dbSNP |
14 | g.23416167A>T | CA389037629 | MHRT,MYH7 | c.4790T>A (p.Leu1597Gln) n.428A>T | |
14 | g.23416168G>A | CA485766545 | MHRT,MYH7 | c.4789C>T (p.Leu1597=) n.429G>A | ClinVar dbSNP |
14 | g.23416168G>C | CA389037630 | MHRT,MYH7 | c.4789C>G (p.Leu1597Val) n.429G>C | |
14 | g.23416168G= | CA2123465611 | MHRT,MYH7 | c.4789C= (p.Leu1597=) n.429G= | |
14 | g.23416168G>T | CA389037631 | MHRT,MYH7 | c.4789C>A (p.Leu1597Met) n.429G>T | |
14 | g.23416169C>A | CA485766546 | MHRT,MYH7 | c.4788G>T (p.Ser1596=) n.430C>A | ClinVar |
14 | g.23416169C= | CA2123465619 | MHRT,MYH7 | c.4788G= (p.Ser1596=) n.430C= | |
14 | g.23416169C>G | CA485766547 | MHRT,MYH7 | c.4788G>C (p.Ser1596=) n.430C>G | ClinVar dbSNP gnomAD v2 gnomAD v4 |
14 | g.23416169C>T | CA015299 | MHRT,MYH7 | c.4788G>A (p.Ser1596=) n.430C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.23416170G>A | CA043848 | MHRT,MYH7 | c.4787C>T (p.Ser1596Leu) n.431G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.23416170G>C | CA389037633 | MHRT,MYH7 | c.4787C>G (p.Ser1596Trp) n.431G>C | |
14 | g.23416170G= | CA2123465623 | MHRT,MYH7 | c.4787C= (p.Ser1596=) n.431G= | |
14 | g.23416170G>T | CA389037632 | MHRT,MYH7 | c.4787C>A (p.Ser1596Ter) n.431G>T | |
14 | g.23416171A= | CA2123465630 | MHRT,MYH7 | c.4786T= (p.Ser1596=) n.432A= | |
14 | g.23416171A>C | CA389037634 | MHRT,MYH7 | c.4786T>G (p.Ser1596Ala) n.432A>C | |
14 | g.23416171A>G | CA043838 | MHRT,MYH7 | c.4786T>C (p.Ser1596Pro) n.432A>G | dbSNP ExAC gnomAD v2 |
14 | g.23416171A>T | CA389037635 | MHRT,MYH7 | c.4786T>A (p.Ser1596Thr) n.432A>T | |
14 | g.23416172G>A | CA485766548 | MHRT,MYH7 | c.4785C>T (p.Asp1595=) n.433G>A | dbSNP gnomAD v2 gnomAD v4 |
14 | g.23416172G>C | CA389037636 | MHRT,MYH7 | c.4785C>G (p.Asp1595Glu) n.433G>C | |
14 | g.23416172G= | CA2123465633 | MHRT,MYH7 | c.4785C= (p.Asp1595=) n.433G= | |
14 | g.23416172G>T | CA389037637 | MHRT,MYH7 | c.4785C>A (p.Asp1595Glu) n.433G>T | |
14 | g.23416173T>A | CA389037638 | MHRT,MYH7 | c.4784A>T (p.Asp1595Val) n.434T>A | |
14 | g.23416173T>C | CA389037639 | MHRT,MYH7 | c.4784A>G (p.Asp1595Gly) n.434T>C | |
14 | g.23416173T>G | CA389037640 | MHRT,MYH7 | c.4784A>C (p.Asp1595Ala) n.434T>G | |
14 | g.23416174C>A | CA389037641 | MHRT,MYH7 | c.4783G>T (p.Asp1595Tyr) n.435C>A | |
14 | g.23416174C= | CA2123465636 | MHRT,MYH7 | c.4783G= (p.Asp1595=) n.435C= | |
14 | g.23416174C>G | CA389037642 | MHRT,MYH7 | c.4783G>C (p.Asp1595His) n.435C>G | |
14 | g.23416174C>T | CA389037643 | MHRT,MYH7 | c.4783G>A (p.Asp1595Asn) n.435C>T | ClinVar dbSNP |
14 | g.23416175C>A | CA485766549 | MHRT,MYH7 | c.4782G>T (p.Val1594=) n.436C>A | |
14 | g.23416175C>G | CA485766550 | MHRT,MYH7 | c.4782G>C (p.Val1594=) n.436C>G | |
14 | g.23416175C>T | CA485766551 | MHRT,MYH7 | c.4782G>A (p.Val1594=) n.436C>T | |
14 | g.23416176A= | CA2123465652 | MHRT,MYH7 | c.4781T= (p.Val1594=) n.437A= | |
14 | g.23416176A>C | CA389037644 | MHRT,MYH7 | c.4781T>G (p.Val1594Gly) n.437A>C | dbSNP |
14 | g.23416176A>G | CA389037645 | MHRT,MYH7 | c.4781T>C (p.Val1594Ala) n.437A>G | |
14 | g.23416176A>T | CA389037646 | MHRT,MYH7 | c.4781T>A (p.Val1594Glu) n.437A>T | |
14 | g.23416177C>A | CA389037648 | MHRT,MYH7 | c.4780G>T (p.Val1594Leu) n.438C>A | gnomAD v4 |
14 | g.23416177C= | CA2123465657 | MHRT,MYH7 | c.4780G= (p.Val1594=) n.438C= | |
14 | g.23416177C>G | CA043815 | MHRT,MYH7 | c.4780G>C (p.Val1594Leu) n.438C>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
14 | g.23416177C>T | CA389037647 | MHRT,MYH7 | c.4780G>A (p.Val1594Met) n.438C>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |
14 | g.23416178C>A | CA485766552 | MHRT,MYH7 | c.4779G>T (p.Val1593=) n.439C>A | gnomAD v4 |
14 | g.23416178C= | CA2123465662 | MHRT,MYH7 | c.4779G= (p.Val1593=) n.439C= | |
14 | g.23416178C>G | CA485766553 | MHRT,MYH7 | c.4779G>C (p.Val1593=) n.439C>G | dbSNP |
14 | g.23416178C>T | CA485766554 | MHRT,MYH7 | c.4779G>A (p.Val1593=) n.439C>T | |
14 | g.23416179A>C | CA389037649 | MHRT,MYH7 | c.4778T>G (p.Val1593Gly) n.440A>C | |
14 | g.23416179A>G | CA389037650 | MHRT,MYH7 | c.4778T>C (p.Val1593Ala) n.440A>G | |
14 | g.23416179A>T | CA389037651 | MHRT,MYH7 | c.4778T>A (p.Val1593Glu) n.440A>T | |
14 | g.23416180C>A | CA389037652 | MHRT,MYH7 | c.4777G>T (p.Val1593Leu) n.441C>A | ClinVar |
14 | g.23416180C>G | CA389037653 | MHRT,MYH7 | c.4777G>C (p.Val1593Leu) n.441C>G | |
14 | g.23416180C>T | CA389037654 | MHRT,MYH7 | c.4777G>A (p.Val1593Met) n.441C>T | gnomAD v4 |
14 | g.23416181C>A | CA485766555 | MHRT,MYH7 | c.4776G>T (p.Arg1592=) n.442C>A | COSMIC |
14 | g.23416181C= | CA2123465669 | MHRT,MYH7 | c.4776G= (p.Arg1592=) n.442C= | |
14 | g.23416181C>G | CA485766556 | MHRT,MYH7 | c.4776G>C (p.Arg1592=) n.442C>G | dbSNP |
14 | g.23416181C>T | CA485766557 | MHRT,MYH7 | c.4776G>A (p.Arg1592=) n.442C>T | |
14 | g.23416182C>A | CA389037655 | MHRT,MYH7 | c.4775G>T (p.Arg1592Leu) n.443C>A | dbSNP gnomAD v4 |
14 | g.23416182C= | CA2123465676 | MHRT,MYH7 | c.4775G= (p.Arg1592=) n.443C= | |
14 | g.23416182C>G | CA389037656 | MHRT,MYH7 | c.4775G>C (p.Arg1592Pro) n.443C>G | |
14 | g.23416182C>T | CA389037657 | MHRT,MYH7 | c.4775G>A (p.Arg1592Gln) n.443C>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.23416183G>A | CA389037658 | MHRT,MYH7 | c.4774C>T (p.Arg1592Trp) n.444G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC |
14 | g.23416183G>C | CA389037659 | MHRT,MYH7 | c.4774C>G (p.Arg1592Gly) n.444G>C | |
14 | g.23416183G= | CA2123465685 | MHRT,MYH7 | c.4774C= (p.Arg1592=) n.444G= | |
14 | g.23416183G>T | CA485766558 | MHRT,MYH7 | c.4774C>A (p.Arg1592=) n.444G>T |