| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 14 | g.23415729_23415731del | CA1139532448 | MHRT,MYH7 | c.5059_5061del (p.Glu1687del) n.161_163del | |
| 14 | g.23415731C>A | CA485766149 | MHRT,MYH7 | c.5055G>T (p.Leu1685=) n.163C>A | dbSNP gnomAD v4 |
| 14 | g.23415731C= | CA2123464248 | MHRT,MYH7 | c.5055G= (p.Leu1685=) n.163C= | |
| 14 | g.23415731C>G | CA485766152 | MHRT,MYH7 | c.5055G>C (p.Leu1685=) n.163C>G | |
| 14 | g.23415731C>T | CA485766150 | MHRT,MYH7 | c.5055G>A (p.Leu1685=) n.163C>T | gnomAD v4 |
| 14 | g.23415732A= | CA2123464255 | MHRT,MYH7 | c.5054T= (p.Leu1685=) n.164A= | |
| 14 | g.23415732A>C | CA389037055 | MHRT,MYH7 | c.5054T>G (p.Leu1685Arg) n.164A>C | |
| 14 | g.23415732A>G | CA389037056 | MHRT,MYH7 | c.5054T>C (p.Leu1685Pro) n.164A>G | |
| 14 | g.23415732A>T | CA045149 | MHRT,MYH7 | c.5054T>A (p.Leu1685Gln) n.164A>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.23415733G>A | CA045144 | MHRT,MYH7 | c.5053C>T (p.Leu1685=) n.165G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.23415733G>C | CA389037057 | MHRT,MYH7 | c.5053C>G (p.Leu1685Val) n.165G>C | |
| 14 | g.23415733G= | CA2123464260 | MHRT,MYH7 | c.5053C= (p.Leu1685=) n.165G= | |
| 14 | g.23415733G>T | CA389037058 | MHRT,MYH7 | c.5053C>A (p.Leu1685Met) n.165G>T | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.23415734C>A | CA389037059 | MHRT,MYH7 | c.5052G>T (p.Glu1684Asp) n.166C>A | |
| 14 | g.23415734C>G | CA389037060 | MHRT,MYH7 | c.5052G>C (p.Glu1684Asp) n.166C>G | |
| 14 | g.23415734C>T | CA485766160 | MHRT,MYH7 | c.5052G>A (p.Glu1684=) n.166C>T | |
| 14 | g.23415735T>A | CA389037061 | MHRT,MYH7 | c.5051A>T (p.Glu1684Val) n.167T>A | |
| 14 | g.23415735T>C | CA389037062 | MHRT,MYH7 | c.5051A>G (p.Glu1684Gly) n.167T>C | |
| 14 | g.23415735T>G | CA389037063 | MHRT,MYH7 | c.5051A>C (p.Glu1684Ala) n.167T>G | |
| 14 | g.23415736C>A | CA389037065 | MHRT,MYH7 | c.5050G>T (p.Glu1684Ter) n.168C>A | |
| 14 | g.23415736C>G | CA389037066 | MHRT,MYH7 | c.5050G>C (p.Glu1684Gln) n.168C>G | |
| 14 | g.23415736C>T | CA389037064 | MHRT,MYH7 | c.5050G>A (p.Glu1684Lys) n.168C>T | COSMIC |
| 14 | g.23415737A= | CA2123464262 | MHRT,MYH7 | c.5049T= (p.Ala1683=) n.169A= | |
| 14 | g.23415737A>C | CA485766164 | MHRT,MYH7 | c.5049T>G (p.Ala1683=) n.169A>C | dbSNP |
| 14 | g.23415737A>G | CA485766168 | MHRT,MYH7 | c.5049T>C (p.Ala1683=) n.169A>G | |
| 14 | g.23415737A>T | CA485766167 | MHRT,MYH7 | c.5049T>A (p.Ala1683=) n.169A>T | |
| 14 | g.23415738G>A | CA389037067 | MHRT,MYH7 | c.5048C>T (p.Ala1683Val) n.170G>A | dbSNP gnomAD v4 |
| 14 | g.23415738G>C | CA389037068 | MHRT,MYH7 | c.5048C>G (p.Ala1683Gly) n.170G>C | |
| 14 | g.23415738G= | CA2123464265 | MHRT,MYH7 | c.5048C= (p.Ala1683=) n.170G= | |
| 14 | g.23415738G>T | CA389037069 | MHRT,MYH7 | c.5048C>A (p.Ala1683Asp) n.170G>T | |
| 14 | g.23415739C>A | CA389037070 | MHRT,MYH7 | c.5047G>T (p.Ala1683Ser) n.171C>A | |
| 14 | g.23415739C>G | CA389037071 | MHRT,MYH7 | c.5047G>C (p.Ala1683Pro) n.171C>G | |
| 14 | g.23415739C>T | CA389037072 | MHRT,MYH7 | c.5047G>A (p.Ala1683Thr) n.171C>T | |
| 14 | g.23415740C>A | CA389037074 | MHRT,MYH7 | c.5046G>T (p.Gln1682His) n.172C>A | ClinVar dbSNP gnomAD v4 |
| 14 | g.23415740C>G | CA389037073 | MHRT,MYH7 | c.5046G>C (p.Gln1682His) n.172C>G | |
| 14 | g.23415740C>T | CA485766171 | MHRT,MYH7 | c.5046G>A (p.Gln1682=) n.172C>T | |
| 14 | g.23415741T>A | CA389037075 | MHRT,MYH7 | c.5045A>T (p.Gln1682Leu) n.173T>A | |
| 14 | g.23415741T>C | CA389037076 | MHRT,MYH7 | c.5045A>G (p.Gln1682Arg) n.173T>C | |
| 14 | g.23415741T>G | CA389037077 | MHRT,MYH7 | c.5045A>C (p.Gln1682Pro) n.173T>G | |
| 14 | g.23415742G>A | CA389037078 | MHRT,MYH7 | c.5044C>T (p.Gln1682Ter) n.174G>A | |
| 14 | g.23415742G>C | CA389037079 | MHRT,MYH7 | c.5044C>G (p.Gln1682Glu) n.174G>C | |
| 14 | g.23415742G>T | CA389037080 | MHRT,MYH7 | c.5044C>A (p.Gln1682Lys) n.174G>T | |
| 14 | g.23415743C>A | CA485766178 | MHRT,MYH7 | c.5043G>T (p.Leu1681=) n.175C>A | |
| 14 | g.23415743C>G | CA485766179 | MHRT,MYH7 | c.5043G>C (p.Leu1681=) n.175C>G | |
| 14 | g.23415743C>T | CA485766180 | MHRT,MYH7 | c.5043G>A (p.Leu1681=) n.175C>T | |
| 14 | g.23415744A>C | CA389037081 | MHRT,MYH7 | c.5042T>G (p.Leu1681Arg) n.176A>C | |
| 14 | g.23415744A>G | CA389037083 | MHRT,MYH7 | c.5042T>C (p.Leu1681Pro) n.176A>G | |
| 14 | g.23415744A>T | CA389037082 | MHRT,MYH7 | c.5042T>A (p.Leu1681Gln) n.176A>T | |
| 14 | g.23415744_23415747dup | CA2575486384 | MHRT,MYH7 | c.5039_5042dup (p.Gln1682AlafsTer4) n.176_179dup | |
| 14 | g.23415745G>A | CA485766181 | MHRT,MYH7 | c.5041C>T (p.Leu1681=) n.177G>A | COSMIC |
| 14 | g.23415745G>C | CA389037084 | MHRT,MYH7 | c.5041C>G (p.Leu1681Val) n.177G>C | dbSNP |
| 14 | g.23415745G= | CA2123464268 | MHRT,MYH7 | c.5041C= (p.Leu1681=) n.177G= | |
| 14 | g.23415745G>T | CA389037085 | MHRT,MYH7 | c.5041C>A (p.Leu1681Met) n.177G>T | |
| 14 | g.23415746C>A | CA485766188 | MHRT,MYH7 | c.5040G>T (p.Leu1680=) n.178C>A | |
| 14 | g.23415746C= | CA2123464269 | MHRT,MYH7 | c.5040G= (p.Leu1680=) n.178C= | |
| 14 | g.23415746C>G | CA485766186 | MHRT,MYH7 | c.5040G>C (p.Leu1680=) n.178C>G | |
| 14 | g.23415746C>T | CA045132 | MHRT,MYH7 | c.5040G>A (p.Leu1680=) n.178C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23415747A= | CA2123464273 | MHRT,MYH7 | c.5039T= (p.Leu1680=) n.179A= | |
| 14 | g.23415747A>C | CA389037086 | MHRT,MYH7 | c.5039T>G (p.Leu1680Arg) n.179A>C | |
| 14 | g.23415747A>G | CA045118 | MHRT,MYH7 | c.5039T>C (p.Leu1680Pro) n.179A>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.23415747A>T | CA389037087 | MHRT,MYH7 | c.5039T>A (p.Leu1680Gln) n.179A>T | |
| 14 | g.23415748G>A | CA485766189 | MHRT,MYH7 | c.5038C>T (p.Leu1680=) n.180G>A | |
| 14 | g.23415748G>C | CA389037088 | MHRT,MYH7 | c.5038C>G (p.Leu1680Val) n.180G>C | |
| 14 | g.23415748G>T | CA389037089 | MHRT,MYH7 | c.5038C>A (p.Leu1680Met) n.180G>T | |
| 14 | g.23415749G>A | CA485766191 | MHRT,MYH7 | c.5037C>T (p.Asn1679=) n.181G>A | dbSNP gnomAD v4 |
| 14 | g.23415749G>C | CA389037090 | MHRT,MYH7 | c.5037C>G (p.Asn1679Lys) n.181G>C | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23415749G= | CA2123464284 | MHRT,MYH7 | c.5037C= (p.Asn1679=) n.181G= | |
| 14 | g.23415749G>T | CA389037091 | MHRT,MYH7 | c.5037C>A (p.Asn1679Lys) n.181G>T | ClinVar dbSNP gnomAD v4 |
| 14 | g.23415750T>A | CA389037093 | MHRT,MYH7 | c.5036A>T (p.Asn1679Ile) n.182T>A | |
| 14 | g.23415750T>C | CA045106 | MHRT,MYH7 | c.5036A>G (p.Asn1679Ser) n.182T>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.23415750T>G | CA389037092 | MHRT,MYH7 | c.5036A>C (p.Asn1679Thr) n.182T>G | dbSNP |
| 14 | g.23415750T= | CA2123464290 | MHRT,MYH7 | c.5036A= (p.Asn1679=) n.182T= | |
| 14 | g.23415751T>A | CA389037094 | MHRT,MYH7 | c.5035A>T (p.Asn1679Tyr) n.183T>A | |
| 14 | g.23415751T>C | CA389037096 | MHRT,MYH7 | c.5035A>G (p.Asn1679Asp) n.183T>C | gnomAD v4 |
| 14 | g.23415751T>G | CA389037095 | MHRT,MYH7 | c.5035A>C (p.Asn1679His) n.183T>G | dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23415751T= | CA2123464293 | MHRT,MYH7 | c.5035A= (p.Asn1679=) n.183T= | |
| 14 | g.23415752G>A | CA045078 | MHRT,MYH7 | c.5034C>T (p.Asn1678=) n.184G>A | dbSNP ExAC gnomAD v3 gnomAD v4 |
| 14 | g.23415752G>C | CA389037098 | MHRT,MYH7 | c.5034C>G (p.Asn1678Lys) n.184G>C | ClinVar |
| 14 | g.23415752G= | CA2123464298 | MHRT,MYH7 | c.5034C= (p.Asn1678=) n.184G= | |
| 14 | g.23415752G>T | CA389037097 | MHRT,MYH7 | c.5034C>A (p.Asn1678Lys) n.184G>T | |
| 14 | g.23415753T>A | CA389037099 | MHRT,MYH7 | c.5033A>T (p.Asn1678Ile) n.185T>A | |
| 14 | g.23415753T>C | CA389037100 | MHRT,MYH7 | c.5033A>G (p.Asn1678Ser) n.185T>C | |
| 14 | g.23415753T>G | CA389037101 | MHRT,MYH7 | c.5033A>C (p.Asn1678Thr) n.185T>G | |
| 14 | g.23415754T>A | CA389037102 | MHRT,MYH7 | c.5032A>T (p.Asn1678Tyr) n.186T>A | gnomAD v4 |
| 14 | g.23415754T>C | CA389037103 | MHRT,MYH7 | c.5032A>G (p.Asn1678Asp) n.186T>C | |
| 14 | g.23415754T>G | CA045048 | MHRT,MYH7 | c.5032A>C (p.Asn1678His) n.186T>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23415754T= | CA2123464301 | MHRT,MYH7 | c.5032A= (p.Asn1678=) n.186T= | |
| 14 | g.23415755G>A | CA485766203 | MHRT,MYH7 | c.5031C>T (p.Arg1677=) n.187G>A | gnomAD v4 |
| 14 | g.23415755G>C | CA485766205 | MHRT,MYH7 | c.5031C>G (p.Arg1677=) n.187G>C | |
| 14 | g.23415755G>T | CA485766206 | MHRT,MYH7 | c.5031C>A (p.Arg1677=) n.187G>T | |
| 14 | g.23415756C>A | CA389037104 | MHRT,MYH7 | c.5030G>T (p.Arg1677Leu) n.188C>A | gnomAD v4 |
| 14 | g.23415756C= | CA2123464308 | MHRT,MYH7 | c.5030G= (p.Arg1677=) n.188C= | |
| 14 | g.23415756C>G | CA389037105 | MHRT,MYH7 | c.5030G>C (p.Arg1677Pro) n.188C>G | ClinVar |
| 14 | g.23415756C>T | CA015595 | MHRT,MYH7 | c.5030G>A (p.Arg1677His) n.188C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 14 | g.23415757G>A | CA015584 | MHRT,MYH7 | c.5029C>T (p.Arg1677Cys) n.189G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.23415757G>C | CA389037106 | MHRT,MYH7 | c.5029C>G (p.Arg1677Gly) n.189G>C | |
| 14 | g.23415757G= | CA2123464318 | MHRT,MYH7 | c.5029C= (p.Arg1677=) n.189G= | |
| 14 | g.23415757G>T | CA389037107 | MHRT,MYH7 | c.5029C>A (p.Arg1677Ser) n.189G>T | |
| 14 | g.23415758C>A | CA485766208 | MHRT,MYH7 | c.5028G>T (p.Arg1676=) n.190C>A | |
| 14 | g.23415758C>G | CA485766209 | MHRT,MYH7 | c.5028G>C (p.Arg1676=) n.190C>G | |
| 14 | g.23415758C>T | CA485766210 | MHRT,MYH7 | c.5028G>A (p.Arg1676=) n.190C>T | |
| 14 | g.23415759C>A | CA389037110 | MHRT,MYH7 | c.5027G>T (p.Arg1676Leu) n.191C>A | |
| 14 | g.23415759C= | CA2123464324 | MHRT,MYH7 | c.5027G= (p.Arg1676=) n.191C= | |
| 14 | g.23415759C>G | CA389037109 | MHRT,MYH7 | c.5027G>C (p.Arg1676Pro) n.191C>G | |
| 14 | g.23415759C>T | CA389037108 | MHRT,MYH7 | c.5027G>A (p.Arg1676Gln) n.191C>T | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.23415760G>A | CA044958 | MHRT,MYH7 | c.5026C>T (p.Arg1676Trp) n.192G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 14 | g.23415760G>C | CA389037111 | MHRT,MYH7 | c.5026C>G (p.Arg1676Gly) n.192G>C | |
| 14 | g.23415760G= | CA2123464332 | MHRT,MYH7 | c.5026C= (p.Arg1676=) n.192G= | |
| 14 | g.23415760G>T | CA485766217 | MHRT,MYH7 | c.5026C>A (p.Arg1676=) n.192G>T | |
| 14 | g.23415761C>A | CA389037112 | MHRT,MYH7 | c.5025G>T (p.Glu1675Asp) n.193C>A | |
| 14 | g.23415761C>G | CA389037113 | MHRT,MYH7 | c.5025G>C (p.Glu1675Asp) n.193C>G | |
| 14 | g.23415761C>T | CA485766219 | MHRT,MYH7 | c.5025G>A (p.Glu1675=) n.193C>T | |
| 14 | g.23415762T>A | CA389037114 | MHRT,MYH7 | c.5024A>T (p.Glu1675Val) n.194T>A | |
| 14 | g.23415762T>C | CA389037115 | MHRT,MYH7 | c.5024A>G (p.Glu1675Gly) n.194T>C | gnomAD v4 |
| 14 | g.23415762T>G | CA389037116 | MHRT,MYH7 | c.5024A>C (p.Glu1675Ala) n.194T>G | |
| 14 | g.23415763C>A | CA389037117 | MHRT,MYH7 | c.5023G>T (p.Glu1675Ter) n.195C>A | |
| 14 | g.23415763C>G | CA389037118 | MHRT,MYH7 | c.5023G>C (p.Glu1675Gln) n.195C>G | |
| 14 | g.23415763C>T | CA389037119 | MHRT,MYH7 | c.5023G>A (p.Glu1675Lys) n.195C>T | |
| 14 | g.23415764C>A | CA485766226 | MHRT,MYH7 | c.5022G>T (p.Val1674=) n.196C>A | |
| 14 | g.23415764C>G | CA485766227 | MHRT,MYH7 | c.5022G>C (p.Val1674=) n.196C>G | |
| 14 | g.23415764C>T | CA485766228 | MHRT,MYH7 | c.5022G>A (p.Val1674=) n.196C>T | |
| 14 | g.23415765A>C | CA389037120 | MHRT,MYH7 | c.5021T>G (p.Val1674Gly) n.197A>C | |
| 14 | g.23415765A>G | CA389037121 | MHRT,MYH7 | c.5021T>C (p.Val1674Ala) n.197A>G | |
| 14 | g.23415765A>T | CA389037122 | MHRT,MYH7 | c.5021T>A (p.Val1674Glu) n.197A>T | ClinVar dbSNP |
| 14 | g.23415765_23415771delinsACGATGG | CA2123464339 | MHRT,MYH7 | c.5015_5021delinsCCATCGT (p.Ala1672=) n.197_203delinsACGATGG | |
| 14 | g.23415766C>A | CA389037124 | MHRT,MYH7 | c.5020G>T (p.Val1674Leu) n.198C>A | ClinVar dbSNP gnomAD v4 |
| 14 | g.23415766C= | CA2123464350 | MHRT,MYH7 | c.5020G= (p.Val1674=) n.198C= | |
| 14 | g.23415766C>G | CA389037123 | MHRT,MYH7 | c.5020G>C (p.Val1674Leu) n.198C>G | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23415766C>T | CA015575 | MHRT,MYH7 | c.5020G>A (p.Val1674Met) n.198C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23415771_23415776del | CA015559 | MHRT,MYH7 | c.5015_5020del (p.Ala1672_Ile1673del) n.203_208del | ClinVar dbSNP |
| 14 | g.23415767G>A | CA044845 | MHRT,MYH7 | c.5019C>T (p.Ile1673=) n.199G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23415767G>C | CA389037125 | MHRT,MYH7 | c.5019C>G (p.Ile1673Met) n.199G>C | gnomAD v4 |
| 14 | g.23415767G= | CA2123464368 | MHRT,MYH7 | c.5019C= (p.Ile1673=) n.199G= | |
| 14 | g.23415767G>T | CA485766234 | MHRT,MYH7 | c.5019C>A (p.Ile1673=) n.199G>T | |
| 14 | g.23415768A>C | CA389037126 | MHRT,MYH7 | c.5018T>G (p.Ile1673Ser) n.200A>C | |
| 14 | g.23415768A>G | CA389037127 | MHRT,MYH7 | c.5018T>C (p.Ile1673Thr) n.200A>G | |
| 14 | g.23415768A>T | CA389037128 | MHRT,MYH7 | c.5018T>A (p.Ile1673Asn) n.200A>T | |
| 14 | g.23415769T>A | CA015565 | MHRT,MYH7 | c.5017A>T (p.Ile1673Phe) n.201T>A | ClinVar dbSNP |
| 14 | g.23415769T>C | CA044805 | MHRT,MYH7 | c.5017A>G (p.Ile1673Val) n.201T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.23415769T>G | CA389037129 | MHRT,MYH7 | c.5017A>C (p.Ile1673Leu) n.201T>G | |
| 14 | g.23415769T= | CA2123464374 | MHRT,MYH7 | c.5017A= (p.Ile1673=) n.201T= | |
| 14 | g.23415770G>A | CA485766239 | MHRT,MYH7 | c.5016C>T (p.Ala1672=) n.202G>A | |
| 14 | g.23415770G>C | CA485766242 | MHRT,MYH7 | c.5016C>G (p.Ala1672=) n.202G>C | ClinVar gnomAD v4 |
| 14 | g.23415770G= | CA2123464379 | MHRT,MYH7 | c.5016C= (p.Ala1672=) n.202G= | |
| 14 | g.23415770G>T | CA257809940 | MHRT,MYH7 | c.5016C>A (p.Ala1672=) n.202G>T | dbSNP |
| 14 | g.23415771G>A | CA389037130 | MHRT,MYH7 | c.5015C>T (p.Ala1672Val) n.203G>A | ClinVar dbSNP gnomAD v4 |
| 14 | g.23415771G>C | CA389037131 | MHRT,MYH7 | c.5015C>G (p.Ala1672Gly) n.203G>C | |
| 14 | g.23415771G>T | CA389037132 | MHRT,MYH7 | c.5015C>A (p.Ala1672Asp) n.203G>T | |
| 14 | g.23415772C>A | CA389037133 | MHRT,MYH7 | c.5014G>T (p.Ala1672Ser) n.204C>A | |
| 14 | g.23415772C= | CA2123464388 | MHRT,MYH7 | c.5014G= (p.Ala1672=) n.204C= | |
| 14 | g.23415772C>G | CA389037134 | MHRT,MYH7 | c.5014G>C (p.Ala1672Pro) n.204C>G | |
| 14 | g.23415772C>T | CA044783 | MHRT,MYH7 | c.5014G>A (p.Ala1672Thr) n.204C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23415773G>A | CA044766 | MHRT,MYH7 | c.5013C>T (p.Ile1671=) n.205G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
| 14 | g.23415773G>C | CA044755 | MHRT,MYH7 | c.5013C>G (p.Ile1671Met) n.205G>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23415773G= | CA2123464400 | MHRT,MYH7 | c.5013C= (p.Ile1671=) n.205G= | |
| 14 | g.23415773G>T | CA485766247 | MHRT,MYH7 | c.5013C>A (p.Ile1671=) n.205G>T | |
| 14 | g.23415774A= | CA2123464404 | MHRT,MYH7 | c.5012T= (p.Ile1671=) n.206A= | |
| 14 | g.23415774A>C | CA389037135 | MHRT,MYH7 | c.5012T>G (p.Ile1671Ser) n.206A>C | |
| 14 | g.23415774A>G | CA015551 | MHRT,MYH7 | c.5012T>C (p.Ile1671Thr) n.206A>G | dbSNP |
| 14 | g.23415774A>T | CA389037136 | MHRT,MYH7 | c.5012T>A (p.Ile1671Asn) n.206A>T | |
| 14 | g.23415775T>A | CA389037137 | MHRT,MYH7 | c.5011A>T (p.Ile1671Phe) n.207T>A | |
| 14 | g.23415775T>C | CA389037138 | MHRT,MYH7 | c.5011A>G (p.Ile1671Val) n.207T>C | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23415775T>G | CA389037139 | MHRT,MYH7 | c.5011A>C (p.Ile1671Leu) n.207T>G | ClinVar dbSNP |
| 14 | g.23415775T= | CA2123464413 | MHRT,MYH7 | c.5011A= (p.Ile1671=) n.207T= | |
| 14 | g.23415776G>A | CA044742 | MHRT,MYH7 | c.5010C>T (p.Asn1670=) n.208G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23415776G>C | CA389037140 | MHRT,MYH7 | c.5010C>G (p.Asn1670Lys) n.208G>C | |
| 14 | g.23415776G= | CA2123464425 | MHRT,MYH7 | c.5010C= (p.Asn1670=) n.208G= | |
| 14 | g.23415776G>T | CA389037141 | MHRT,MYH7 | c.5010C>A (p.Asn1670Lys) n.208G>T | |
| 14 | g.23415777T>A | CA389037142 | MHRT,MYH7 | c.5009A>T (p.Asn1670Ile) n.209T>A | |
| 14 | g.23415777T>C | CA389037143 | MHRT,MYH7 | c.5009A>G (p.Asn1670Ser) n.209T>C | |
| 14 | g.23415777T>G | CA389037144 | MHRT,MYH7 | c.5009A>C (p.Asn1670Thr) n.209T>G | |
| 14 | g.23415778T>A | CA389037146 | MHRT,MYH7 | c.5008A>T (p.Asn1670Tyr) n.210T>A | |
| 14 | g.23415778T>C | CA389037147 | MHRT,MYH7 | c.5008A>G (p.Asn1670Asp) n.210T>C | |
| 14 | g.23415778T>G | CA389037145 | MHRT,MYH7 | c.5008A>C (p.Asn1670His) n.210T>G | |
| 14 | g.23415778_23415781delinsTCTC | CA2123464428 | MHRT,MYH7 | c.5005_5008delinsGAGA (p.Glu1669=) n.210_213delinsTCTC | |
| 14 | g.23415779C>A | CA389037148 | MHRT,MYH7 | c.5007G>T (p.Glu1669Asp) n.211C>A | |
| 14 | g.23415779C>G | CA389037149 | MHRT,MYH7 | c.5007G>C (p.Glu1669Asp) n.211C>G | |
| 14 | g.23415779C>T | CA485766259 | MHRT,MYH7 | c.5007G>A (p.Glu1669=) n.211C>T | |
| 14 | g.23415781_23415783del | CA015545 | MHRT,MYH7 | c.5005_5007del (p.Glu1669del) n.213_215del | ClinVar dbSNP |
| 14 | g.23415780T>A | CA389037150 | MHRT,MYH7 | c.5006A>T (p.Glu1669Val) n.212T>A | |
| 14 | g.23415780T>C | CA389037151 | MHRT,MYH7 | c.5006A>G (p.Glu1669Gly) n.212T>C | gnomAD v4 |
| 14 | g.23415780T>G | CA389037152 | MHRT,MYH7 | c.5006A>C (p.Glu1669Ala) n.212T>G | |
| 14 | g.23415781C>A | CA257809989 | MHRT,MYH7 | c.5005G>T (p.Glu1669Ter) n.213C>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23415781C= | CA2123464439 | MHRT,MYH7 | c.5005G= (p.Glu1669=) n.213C= | |
| 14 | g.23415781C>G | CA389037153 | MHRT,MYH7 | c.5005G>C (p.Glu1669Gln) n.213C>G | |
| 14 | g.23415781C>T | CA389037154 | MHRT,MYH7 | c.5005G>A (p.Glu1669Lys) n.213C>T | COSMIC |
| 14 | g.23415782C>A | CA389037155 | MHRT,MYH7 | c.5004G>T (p.Lys1668Asn) n.214C>A | ClinVar |
| 14 | g.23415782C= | CA2123464444 | MHRT,MYH7 | c.5004G= (p.Lys1668=) n.214C= | |
| 14 | g.23415782C>G | CA389037156 | MHRT,MYH7 | c.5004G>C (p.Lys1668Asn) n.214C>G | |
| 14 | g.23415782C>T | CA044704 | MHRT,MYH7 | c.5004G>A (p.Lys1668=) n.214C>T | ClinVar dbSNP ExAC gnomAD v4 COSMIC |
| 14 | g.23415783T>A | CA389037157 | MHRT,MYH7 | c.5003A>T (p.Lys1668Met) n.215T>A | |
| 14 | g.23415783T>C | CA389037158 | MHRT,MYH7 | c.5003A>G (p.Lys1668Arg) n.215T>C | dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23415783T>G | CA389037159 | MHRT,MYH7 | c.5003A>C (p.Lys1668Thr) n.215T>G | |
| 14 | g.23415783T= | CA2123464449 | MHRT,MYH7 | c.5003A= (p.Lys1668=) n.215T= | |
| 14 | g.23415784T>A | CA389037162 | MHRT,MYH7 | c.5002A>T (p.Lys1668Ter) n.216T>A | |
| 14 | g.23415784T>C | CA389037160 | MHRT,MYH7 | c.5002A>G (p.Lys1668Glu) n.216T>C | ClinVar dbSNP |
| 14 | g.23415784T>G | CA389037161 | MHRT,MYH7 | c.5002A>C (p.Lys1668Gln) n.216T>G | |
| 14 | g.23415784T= | CA2123464454 | MHRT,MYH7 | c.5002A= (p.Lys1668=) n.216T= | |
| 14 | g.23415785C>A | CA485766271 | MHRT,MYH7 | c.5001G>T (p.Leu1667=) n.217C>A | |
| 14 | g.23415785C= | CA2123464459 | MHRT,MYH7 | c.5001G= (p.Leu1667=) n.217C= | |
| 14 | g.23415785C>G | CA485766273 | MHRT,MYH7 | c.5001G>C (p.Leu1667=) n.217C>G | |
| 14 | g.23415785C>T | CA485766274 | MHRT,MYH7 | c.5001G>A (p.Leu1667=) n.217C>T | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.23415786A>C | CA389037163 | MHRT,MYH7 | c.5000T>G (p.Leu1667Arg) n.218A>C | |
| 14 | g.23415786A>G | CA389037164 | MHRT,MYH7 | c.5000T>C (p.Leu1667Pro) n.218A>G | |
| 14 | g.23415786A>T | CA389037165 | MHRT,MYH7 | c.5000T>A (p.Leu1667Gln) n.218A>T | |
| 14 | g.23415787G>A | CA485766275 | MHRT,MYH7 | c.4999C>T (p.Leu1667=) n.219G>A | |
| 14 | g.23415787G>C | CA389037166 | MHRT,MYH7 | c.4999C>G (p.Leu1667Val) n.219G>C | |
| 14 | g.23415787G>T | CA389037167 | MHRT,MYH7 | c.4999C>A (p.Leu1667Met) n.219G>T | |
| 14 | g.23415788G>A | CA485766278 | MHRT,MYH7 | c.4998C>T (p.Asp1666=) n.220G>A | |
| 14 | g.23415788G>C | CA389037168 | MHRT,MYH7 | c.4998C>G (p.Asp1666Glu) n.220G>C | |
| 14 | g.23415788G= | CA2123464466 | MHRT,MYH7 | c.4998C= (p.Asp1666=) n.220G= | |
| 14 | g.23415788G>T | CA389037169 | MHRT,MYH7 | c.4998C>A (p.Asp1666Glu) n.220G>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23415789T>A | CA389037170 | MHRT,MYH7 | c.4997A>T (p.Asp1666Val) n.221T>A | |
| 14 | g.23415789T>C | CA389037171 | MHRT,MYH7 | c.4997A>G (p.Asp1666Gly) n.221T>C | |
| 14 | g.23415789T>G | CA389037172 | MHRT,MYH7 | c.4997A>C (p.Asp1666Ala) n.221T>G | |
| 14 | g.23415790C>A | CA389037174 | MHRT,MYH7 | c.4996G>T (p.Asp1666Tyr) n.222C>A | |
| 14 | g.23415790C= | CA2123464476 | MHRT,MYH7 | c.4996G= (p.Asp1666=) n.222C= | |
| 14 | g.23415790C>G | CA389037173 | MHRT,MYH7 | c.4996G>C (p.Asp1666His) n.222C>G | |
| 14 | g.23415790C>T | CA044679 | MHRT,MYH7 | c.4996G>A (p.Asp1666Asn) n.222C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 14 | g.23415791G>A | CA485766283 | MHRT,MYH7 | c.4995C>T (p.Asp1665=) n.223G>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23415791G>C | CA389037175 | MHRT,MYH7 | c.4995C>G (p.Asp1665Glu) n.223G>C | |
| 14 | g.23415791G= | CA2123464487 | MHRT,MYH7 | c.4995C= (p.Asp1665=) n.223G= | |
| 14 | g.23415791G>T | CA389037176 | MHRT,MYH7 | c.4995C>A (p.Asp1665Glu) n.223G>T | |
| 14 | g.23415792T>A | CA389037177 | MHRT,MYH7 | c.4994A>T (p.Asp1665Val) n.224T>A | |
| 14 | g.23415792T>C | CA389037178 | MHRT,MYH7 | c.4994A>G (p.Asp1665Gly) n.224T>C | |
| 14 | g.23415792T>G | CA389037179 | MHRT,MYH7 | c.4994A>C (p.Asp1665Ala) n.224T>G | |
| 14 | g.23415793C>A | CA389037180 | MHRT,MYH7 | c.4993G>T (p.Asp1665Tyr) n.225C>A | |
| 14 | g.23415793C= | CA2123464494 | MHRT,MYH7 | c.4993G= (p.Asp1665=) n.225C= | |
| 14 | g.23415793C>G | CA389037181 | MHRT,MYH7 | c.4993G>C (p.Asp1665His) n.225C>G | |
| 14 | g.23415793C>T | CA044655 | MHRT,MYH7 | c.4993G>A (p.Asp1665Asn) n.225C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
| 14 | g.23415794G>A | CA044648 | MHRT,MYH7 | c.4992C>T (p.Asn1664=) n.226G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 14 | g.23415794G>C | CA389037182 | MHRT,MYH7 | c.4992C>G (p.Asn1664Lys) n.226G>C | |
| 14 | g.23415794G= | CA2123464500 | MHRT,MYH7 | c.4992C= (p.Asn1664=) n.226G= | |
| 14 | g.23415794G>T | CA044638 | MHRT,MYH7 | c.4992C>A (p.Asn1664Lys) n.226G>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.23415795T>A | CA389037185 | MHRT,MYH7 | c.4991A>T (p.Asn1664Ile) n.227T>A | |
| 14 | g.23415795T>C | CA389037184 | MHRT,MYH7 | c.4991A>G (p.Asn1664Ser) n.227T>C | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23415795T>G | CA389037183 | MHRT,MYH7 | c.4991A>C (p.Asn1664Thr) n.227T>G | |
| 14 | g.23415795T= | CA2123464511 | MHRT,MYH7 | c.4991A= (p.Asn1664=) n.227T= | |
| 14 | g.23415796T>A | CA389037186 | MHRT,MYH7 | c.4990A>T (p.Asn1664Tyr) n.228T>A | |
| 14 | g.23415796T>C | CA389037187 | MHRT,MYH7 | c.4990A>G (p.Asn1664Asp) n.228T>C | |
| 14 | g.23415796T>G | CA389037188 | MHRT,MYH7 | c.4990A>C (p.Asn1664His) n.228T>G | |
| 14 | g.23415797G>A | CA485766293 | MHRT,MYH7 | c.4989C>T (p.Ala1663=) n.229G>A | |
| 14 | g.23415797G>C | CA485766294 | MHRT,MYH7 | c.4989C>G (p.Ala1663=) n.229G>C | |
| 14 | g.23415797G>T | CA485766295 | MHRT,MYH7 | c.4989C>A (p.Ala1663=) n.229G>T | |
| 14 | g.23415798G>A | CA389037189 | MHRT,MYH7 | c.4988C>T (p.Ala1663Val) n.230G>A | ClinVar dbSNP |
| 14 | g.23415798G>C | CA389037190 | MHRT,MYH7 | c.4988C>G (p.Ala1663Gly) n.230G>C | |
| 14 | g.23415798G= | CA2123464517 | MHRT,MYH7 | c.4988C= (p.Ala1663=) n.230G= | |
| 14 | g.23415798G>T | CA389037191 | MHRT,MYH7 | c.4988C>A (p.Ala1663Asp) n.230G>T | ClinVar dbSNP |
| 14 | g.23415799C>A | CA389037192 | MHRT,MYH7 | c.4987G>T (p.Ala1663Ser) n.231C>A | |
| 14 | g.23415799C= | CA2123464526 | MHRT,MYH7 | c.4987G= (p.Ala1663=) n.231C= | |
| 14 | g.23415799C>G | CA347268 | MHRT,MYH7 | c.4987G>C (p.Ala1663Pro) n.231C>G | dbSNP |
| 14 | g.23415799C>T | CA389037193 | MHRT,MYH7 | c.4987G>A (p.Ala1663Thr) n.231C>T | ClinVar |
| 14 | g.23415800A>C | CA485766296 | MHRT,MYH7 | c.4986T>G (p.Arg1662=) n.232A>C | |
| 14 | g.23415800A>G | CA485766298 | MHRT,MYH7 | c.4986T>C (p.Arg1662=) n.232A>G | |
| 14 | g.23415800A>T | CA485766300 | MHRT,MYH7 | c.4986T>A (p.Arg1662=) n.232A>T | |
| 14 | g.23415801C>A | CA16614388 | MHRT,MYH7 | c.4985G>T (p.Arg1662Leu) n.233C>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23415801C= | CA2123464538 | MHRT,MYH7 | c.4985G= (p.Arg1662=) n.233C= | |
| 14 | g.23415801C>G | CA015530 | MHRT,MYH7 | c.4985G>C (p.Arg1662Pro) n.233C>G | ClinVar dbSNP |
| 14 | g.23415801C>T | CA015524 | MHRT,MYH7 | c.4985G>A (p.Arg1662His) n.233C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23415802G>A | CA044615 | MHRT,MYH7 | c.4984C>T (p.Arg1662Cys) n.234G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 14 | g.23415802G>C | CA389037195 | MHRT,MYH7 | c.4984C>G (p.Arg1662Gly) n.234G>C | |
| 14 | g.23415802G= | CA2123464553 | MHRT,MYH7 | c.4984C= (p.Arg1662=) n.234G= | |
| 14 | g.23415802G>T | CA389037194 | MHRT,MYH7 | c.4984C>A (p.Arg1662Ser) n.234G>T | |
| 14 | g.23415803G>A | CA485766305 | MHRT,MYH7 | c.4983C>T (p.Val1661=) n.235G>A | |
| 14 | g.23415803G>C | CA485766306 | MHRT,MYH7 | c.4983C>G (p.Val1661=) n.235G>C | |
| 14 | g.23415803G>T | CA485766303 | MHRT,MYH7 | c.4983C>A (p.Val1661=) n.235G>T | |
| 14 | g.23415804A>C | CA389037196 | MHRT,MYH7 | c.4982T>G (p.Val1661Gly) n.236A>C | |
| 14 | g.23415804A>G | CA389037198 | MHRT,MYH7 | c.4982T>C (p.Val1661Ala) n.236A>G | |
| 14 | g.23415804A>T | CA389037197 | MHRT,MYH7 | c.4982T>A (p.Val1661Asp) n.236A>T | |
| 14 | g.23415805del | CA2624233546 | MHRT,MYH7 | c.4981del (p.Val1661SerfsTer7) n.237del | gnomAD v4 |
| 14 | g.23415805C>A | CA389037199 | MHRT,MYH7 | c.4981G>T (p.Val1661Phe) n.237C>A | |
| 14 | g.23415805C= | CA2123464564 | MHRT,MYH7 | c.4981G= (p.Val1661=) n.237C= | |
| 14 | g.23415805C>G | CA389037200 | MHRT,MYH7 | c.4981G>C (p.Val1661Leu) n.237C>G | ClinVar dbSNP |
| 14 | g.23415805C>T | CA389037201 | MHRT,MYH7 | c.4981G>A (p.Val1661Ile) n.237C>T | ClinVar dbSNP gnomAD v4 |
| 14 | g.23415806T>A | CA485766311 | MHRT,MYH7 | c.4980A>T (p.Ala1660=) n.238T>A | |
| 14 | g.23415806T>C | CA044604 | MHRT,MYH7 | c.4980A>G (p.Ala1660=) n.238T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23415806T>G | CA015515 | MHRT,MYH7 | c.4980A>C (p.Ala1660=) n.238T>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23415806T= | CA2123464574 | MHRT,MYH7 | c.4980A= (p.Ala1660=) n.238T= | |
| 14 | g.23415807G>A | CA389037203 | MHRT,MYH7 | c.4979C>T (p.Ala1660Val) n.239G>A | dbSNP |
| 14 | g.23415807G>C | CA389037202 | MHRT,MYH7 | c.4979C>G (p.Ala1660Gly) n.239G>C | |
| 14 | g.23415807G= | CA2123464582 | MHRT,MYH7 | c.4979C= (p.Ala1660=) n.239G= | |
| 14 | g.23415807G>T | CA257810052 | MHRT,MYH7 | c.4979C>A (p.Ala1660Glu) n.239G>T | ClinVar dbSNP gnomAD v4 |
| 14 | g.23415808C>A | CA389037204 | MHRT,MYH7 | c.4978G>T (p.Ala1660Ser) n.240C>A | |
| 14 | g.23415808C= | CA2123464584 | MHRT,MYH7 | c.4978G= (p.Ala1660=) n.240C= | |
| 14 | g.23415808C>G | CA389037205 | MHRT,MYH7 | c.4978G>C (p.Ala1660Pro) n.240C>G | ClinVar dbSNP |
| 14 | g.23415808C>T | CA389037206 | MHRT,MYH7 | c.4978G>A (p.Ala1660Thr) n.240C>T | gnomAD v4 |
| 14 | g.23415809A= | CA2123464589 | MHRT,MYH7 | c.4977T= (p.Asp1659=) n.241A= | |
| 14 | g.23415809A>C | CA389037207 | MHRT,MYH7 | c.4977T>G (p.Asp1659Glu) n.241A>C | |
| 14 | g.23415809A>G | CA044584 | MHRT,MYH7 | c.4977T>C (p.Asp1659=) n.241A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.23415809A>T | CA389037208 | MHRT,MYH7 | c.4977T>A (p.Asp1659Glu) n.241A>T | dbSNP gnomAD v4 |
| 14 | g.23415810T>A | CA389037211 | MHRT,MYH7 | c.4976A>T (p.Asp1659Val) n.242T>A | |
| 14 | g.23415810T>C | CA389037209 | MHRT,MYH7 | c.4976A>G (p.Asp1659Gly) n.242T>C | |
| 14 | g.23415810T>G | CA389037210 | MHRT,MYH7 | c.4976A>C (p.Asp1659Ala) n.242T>G | |
| 14 | g.23415811C>A | CA389037212 | MHRT,MYH7 | c.4975G>T (p.Asp1659Tyr) n.243C>A | dbSNP |
| 14 | g.23415811C= | CA2123464595 | MHRT,MYH7 | c.4975G= (p.Asp1659=) n.243C= | |
| 14 | g.23415811C>G | CA389037213 | MHRT,MYH7 | c.4975G>C (p.Asp1659His) n.243C>G | |
| 14 | g.23415811C>T | CA044566 | MHRT,MYH7 | c.4975G>A (p.Asp1659Asn) n.243C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.23415811_23415812delinsCG | CA2123464599 | MHRT,MYH7 | c.4974_4975delinsCG (p.Asp1658=) n.243_244delinsCG | |
| 14 | g.23415812del | CA2123464604 | MHRT,MYH7 | c.4974del (p.Asp1658GlufsTer10) n.244del | dbSNP |
| 14 | g.23415812G>A | CA015510 | MHRT,MYH7 | c.4974C>T (p.Asp1658=) n.244G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 14 | g.23415812G>C | CA389037214 | MHRT,MYH7 | c.4974C>G (p.Asp1658Glu) n.244G>C | |
| 14 | g.23415812G= | CA2123464606 | MHRT,MYH7 | c.4974C= (p.Asp1658=) n.244G= | |
| 14 | g.23415812G>T | CA389037215 | MHRT,MYH7 | c.4974C>A (p.Asp1658Glu) n.244G>T | |
| 14 | g.23415813T>A | CA389037216 | MHRT,MYH7 | c.4973A>T (p.Asp1658Val) n.245T>A | |
| 14 | g.23415813T>C | CA389037217 | MHRT,MYH7 | c.4973A>G (p.Asp1658Gly) n.245T>C | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23415813T>G | CA389037218 | MHRT,MYH7 | c.4973A>C (p.Asp1658Ala) n.245T>G | |
| 14 | g.23415813T= | CA2123464617 | MHRT,MYH7 | c.4973A= (p.Asp1658=) n.245T= | |
| 14 | g.23415814C>A | CA389037219 | MHRT,MYH7 | c.4972G>T (p.Asp1658Tyr) n.246C>A | |
| 14 | g.23415814C>G | CA389037220 | MHRT,MYH7 | c.4972G>C (p.Asp1658His) n.246C>G | |
| 14 | g.23415814C>T | CA389037221 | MHRT,MYH7 | c.4972G>A (p.Asp1658Asn) n.246C>T | ClinVar |
| 14 | g.23415815C>A | CA485766333 | MHRT,MYH7 | c.4971G>T (p.Leu1657=) n.247C>A | |
| 14 | g.23415815C>G | CA485766329 | MHRT,MYH7 | c.4971G>C (p.Leu1657=) n.247C>G | |
| 14 | g.23415815C>T | CA485766335 | MHRT,MYH7 | c.4971G>A (p.Leu1657=) n.247C>T | |
| 14 | g.23415816A>C | CA389037222 | MHRT,MYH7 | c.4970T>G (p.Leu1657Arg) n.248A>C | |
| 14 | g.23415816A>G | CA389037224 | MHRT,MYH7 | c.4970T>C (p.Leu1657Pro) n.248A>G | ClinVar dbSNP |
| 14 | g.23415816A>T | CA389037223 | MHRT,MYH7 | c.4970T>A (p.Leu1657Gln) n.248A>T | |
| 14 | g.23415817G>A | CA485766338 | MHRT,MYH7 | c.4969C>T (p.Leu1657=) n.249G>A | |
| 14 | g.23415817G>C | CA389037225 | MHRT,MYH7 | c.4969C>G (p.Leu1657Val) n.249G>C | |
| 14 | g.23415817G>T | CA389037226 | MHRT,MYH7 | c.4969C>A (p.Leu1657Met) n.249G>T | |
| 14 | g.23415818C>A | CA389037227 | MHRT,MYH7 | c.4968G>T (p.Gln1656His) n.250C>A | |
| 14 | g.23415818C>G | CA389037228 | MHRT,MYH7 | c.4968G>C (p.Gln1656His) n.250C>G | |
| 14 | g.23415818C>T | CA485766341 | MHRT,MYH7 | c.4968G>A (p.Gln1656=) n.250C>T | |
| 14 | g.23415819T>A | CA389037229 | MHRT,MYH7 | c.4967A>T (p.Gln1656Leu) n.251T>A | |
| 14 | g.23415819T>C | CA389037230 | MHRT,MYH7 | c.4967A>G (p.Gln1656Arg) n.251T>C | |
| 14 | g.23415819T>G | CA389037231 | MHRT,MYH7 | c.4967A>C (p.Gln1656Pro) n.251T>G | |
| 14 | g.23415820G>A | CA389037232 | MHRT,MYH7 | c.4966C>T (p.Gln1656Ter) n.252G>A | ClinVar dbSNP gnomAD v4 |
| 14 | g.23415820G>C | CA389037233 | MHRT,MYH7 | c.4966C>G (p.Gln1656Glu) n.252G>C | ClinVar dbSNP |
| 14 | g.23415820G= | CA2123464632 | MHRT,MYH7 | c.4966C= (p.Gln1656=) n.252G= | |
| 14 | g.23415820G>T | CA389037234 | MHRT,MYH7 | c.4966C>A (p.Gln1656Lys) n.252G>T | |
| 14 | g.23415821A= | CA2123464636 | MHRT,MYH7 | c.4965T= (p.Ile1655=) n.253A= | |
| 14 | g.23415821A>C | CA389037235 | MHRT,MYH7 | c.4965T>G (p.Ile1655Met) n.253A>C | |
| 14 | g.23415821A>G | CA10587765 | MHRT,MYH7 | c.4965T>C (p.Ile1655=) n.253A>G | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23415821A>T | CA485766346 | MHRT,MYH7 | c.4965T>A (p.Ile1655=) n.253A>T | |
| 14 | g.23415822A= | CA2123464639 | MHRT,MYH7 | c.4964T= (p.Ile1655=) n.254A= | |
| 14 | g.23415822A>C | CA389037238 | MHRT,MYH7 | c.4964T>G (p.Ile1655Ser) n.254A>C | |
| 14 | g.23415822A>G | CA389037236 | MHRT,MYH7 | c.4964T>C (p.Ile1655Thr) n.254A>G | ClinVar dbSNP |
| 14 | g.23415822A>T | CA389037237 | MHRT,MYH7 | c.4964T>A (p.Ile1655Asn) n.254A>T | |
| 14 | g.23415823T>A | CA389037239 | MHRT,MYH7 | c.4963A>T (p.Ile1655Phe) n.255T>A | |
| 14 | g.23415823T>C | CA389037240 | MHRT,MYH7 | c.4963A>G (p.Ile1655Val) n.255T>C | |
| 14 | g.23415823T>G | CA389037241 | MHRT,MYH7 | c.4963A>C (p.Ile1655Leu) n.255T>G | |
| 14 | g.23415824C>A | CA389037242 | MHRT,MYH7 | c.4962G>T (p.Gln1654His) n.256C>A | |
| 14 | g.23415824C>G | CA389037243 | MHRT,MYH7 | c.4962G>C (p.Gln1654His) n.256C>G | |
| 14 | g.23415824C>T | CA485766351 | MHRT,MYH7 | c.4962G>A (p.Gln1654=) n.256C>T | |
| 14 | g.23415825T>A | CA389037244 | MHRT,MYH7 | c.4961A>T (p.Gln1654Leu) n.257T>A | |
| 14 | g.23415825T>C | CA389037245 | MHRT,MYH7 | c.4961A>G (p.Gln1654Arg) n.257T>C | COSMIC |
| 14 | g.23415825T>G | CA389037246 | MHRT,MYH7 | c.4961A>C (p.Gln1654Pro) n.257T>G | |
| 14 | g.23415826G>A | CA389037247 | MHRT,MYH7 | c.4960C>T (p.Gln1654Ter) n.258G>A | ClinVar dbSNP |
| 14 | g.23415826G>C | CA389037248 | MHRT,MYH7 | c.4960C>G (p.Gln1654Glu) n.258G>C | |
| 14 | g.23415826G= | CA2123464648 | MHRT,MYH7 | c.4960C= (p.Gln1654=) n.258G= | |
| 14 | g.23415826G>T | CA389037249 | MHRT,MYH7 | c.4960C>A (p.Gln1654Lys) n.258G>T | |
| 14 | g.23415828del | CA2580087965 | MHRT,MYH7 | c.4960del (p.Gln1654ArgfsTer14) n.260del | ClinVar |
| 14 | g.23415827G>A | CA485766357 | MHRT,MYH7 | c.4959C>T (p.Thr1653=) n.259G>A | |
| 14 | g.23415827G>C | CA485766358 | MHRT,MYH7 | c.4959C>G (p.Thr1653=) n.259G>C | |
| 14 | g.23415827G>T | CA485766359 | MHRT,MYH7 | c.4959C>A (p.Thr1653=) n.259G>T | |
| 14 | g.23415828G>A | CA389037252 | MHRT,MYH7 | c.4958C>T (p.Thr1653Ile) n.260G>A | |
| 14 | g.23415828G>C | CA389037251 | MHRT,MYH7 | c.4958C>G (p.Thr1653Ser) n.260G>C | |
| 14 | g.23415828G>T | CA389037250 | MHRT,MYH7 | c.4958C>A (p.Thr1653Asn) n.260G>T | |
| 14 | g.23415831_23415850del | CA2573053877 | MHRT,MYH7 | c.4954-15_4958del n.261+2_261+21del | ClinVar dbSNP |
| 14 | g.23415829T>A | CA389037253 | MHRT,MYH7 | c.4957A>T (p.Thr1653Ser) n.261T>A | |
| 14 | g.23415829T>C | CA389037255 | MHRT,MYH7 | c.4957A>G (p.Thr1653Ala) n.261T>C | |
| 14 | g.23415829T>G | CA389037254 | MHRT,MYH7 | c.4957A>C (p.Thr1653Pro) n.261T>G | |
| 14 | g.23415830G>A | CA485766361 | MHRT,MYH7 | c.4956C>T (p.Asp1652=) n.261+1G>A | |
| 14 | g.23415830G>C | CA389037256 | MHRT,MYH7 | c.4956C>G (p.Asp1652Glu) n.261+1G>C | |
| 14 | g.23415830G>T | CA389037257 | MHRT,MYH7 | c.4956C>A (p.Asp1652Glu) n.261+1G>T | |
| 14 | g.23415831T>A | CA389037258 | MHRT,MYH7 | c.4955A>T (p.Asp1652Val) n.261+2T>A | |
| 14 | g.23415831T>C | CA389037259 | MHRT,MYH7 | c.4955A>G (p.Asp1652Gly) n.261+2T>C | |
| 14 | g.23415831T>G | CA389037260 | MHRT,MYH7 | c.4955A>C (p.Asp1652Ala) n.261+2T>G | ClinVar dbSNP |