UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 12 | g.102865713_102871066del | CA916084429 | PAH | c.442-4403_509+883del c.427-4403_494+883del n.538-4403_605+883del n.530+6396_531-10381del | ClinVar |
| 12 | g.102865820_102866770del | CA16020806 | PAH | c.442-102_509+781del c.427-102_494+781del n.538-102_605+781del n.530+10697_531-10483del | |
| 12 | g.102866372_102868042del | CA916084427 | PAH | c.442-1377_509+226del c.427-1377_494+226del n.538-1377_605+226del n.530+9422_531-11038del | ClinVar |
| 12 | g.102866594_102866662delinsACTGGCGGTAGTTGTAGGCAATGTCAGCAAACTGCTTCCGTCTTGCACGGTACACAGGATCTTTAAAAC | CA2059456968 | PAH | c.443_509+2delinsGTTTTAAAGATCCTGTGTACCGTGCAAGACGGAAGCAGTTTGCTGACATTGCCTACAACTACCGCCAGT c.428_494+2delinsGTTTTAAAGATCCTGTGTACCGTGCAAGACGGAAGCAGTTTGCTGACATTGCCTACAACTACCGCCAGT n.539_605+2delinsGTTTTAAAGATCCTGTGTACCGTGCAAGACGGAAGCAGTTTGCTGACATTGCCTACAACTACCGCCAGT n.530+10800_530+10868delinsGTTTTAAAGATCCTGTGTACCGTGCAAGACGGAAGCAGTTTGCTGACATTGCCTACAACTACCGCCAGT | |
| 12 | g.102866596_102866663del | CA229552 | PAH | c.443_509+1del c.428_494+1del n.539_605+1del n.530+10800_530+10867del | ClinVar dbSNP |
| 12 | g.102866609A>C | CA386299499 | PAH | c.496T>G (p.Tyr166Asp) c.481T>G (p.Tyr161Asp) n.592T>G n.530+10853T>G | |
| 12 | g.102866609A>G | CA386299501 | PAH | c.496T>C (p.Tyr166His) c.481T>C (p.Tyr161His) n.592T>C n.530+10853T>C | |
| 12 | g.102866609A>T | CA386299503 | PAH | c.496T>A (p.Tyr166Asn) c.481T>A (p.Tyr161Asn) n.592T>A n.530+10853T>A | |
| 12 | g.102866610_102866613del | CA2580085681 | PAH | c.493_496del (p.Ala165ThrfsTer29) c.478_481del (p.Ala160ThrfsTer29) n.589_592del n.530+10850_530+10853del | ClinVar |
| 12 | g.102866610G>A | CA481332090 | PAH | c.495C>T (p.Ala165=) c.480C>T (p.Ala160=) n.591C>T n.530+10852C>T | ClinVar dbSNP gnomAD v4 |
| 12 | g.102866610G>C | CA481332091 | PAH | c.495C>G (p.Ala165=) c.480C>G (p.Ala160=) n.591C>G n.530+10852C>G | |
| 12 | g.102866610G= | CA2059456983 | PAH | c.495C= (p.Ala165=) c.480C= (p.Ala160=) n.591C= n.530+10852C= | |
| 12 | g.102866610G>T | CA481332092 | PAH | c.495C>A (p.Ala165=) c.480C>A (p.Ala160=) n.591C>A n.530+10852C>A | |
| 12 | g.102866611G>A | CA386299506 | PAH | c.494C>T (p.Ala165Val) c.479C>T (p.Ala160Val) n.590C>T n.530+10851C>T | gnomAD v4 |
| 12 | g.102866611G>C | CA386299508 | PAH | c.494C>G (p.Ala165Gly) c.479C>G (p.Ala160Gly) n.590C>G n.530+10851C>G | |
| 12 | g.102866611G= | CA2059456984 | PAH | c.494C= (p.Ala165=) c.479C= (p.Ala160=) n.590C= n.530+10851C= | |
| 12 | g.102866611G>T | CA16020800 | PAH | c.494C>A (p.Ala165Asp) c.479C>A (p.Ala160Asp) n.590C>A n.530+10851C>A | ClinVar dbSNP |
| 12 | g.102866611_102866612insA | CA2695217253 | PAH | c.493_494insT (p.Ala165ValfsTer?) c.478_479insT (p.Ala160ValfsTer?) n.589_590insT n.530+10850_530+10851insT | |
| 12 | g.102866612C>A | CA386299512 | PAH | c.493G>T (p.Ala165Ser) c.478G>T (p.Ala160Ser) n.589G>T n.530+10850G>T | |
| 12 | g.102866612C= | CA2059456985 | PAH | c.493G= (p.Ala165=) c.478G= (p.Ala160=) n.589G= n.530+10850G= | |
| 12 | g.102866612C>G | CA229581 | PAH | c.493G>C (p.Ala165Pro) c.478G>C (p.Ala160Pro) n.589G>C n.530+10850G>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 12 | g.102866612C>T | CA229579 | PAH | c.493G>A (p.Ala165Thr) c.478G>A (p.Ala160Thr) n.589G>A n.530+10850G>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.102866613A>C | CA386299515 | PAH | c.492T>G (p.Ile164Met) c.477T>G (p.Ile159Met) n.588T>G n.530+10849T>G | |
| 12 | g.102866613A>G | CA481332093 | PAH | c.492T>C (p.Ile164=) c.477T>C (p.Ile159=) n.588T>C n.530+10849T>C | |
| 12 | g.102866613A>T | CA481332094 | PAH | c.492T>A (p.Ile164=) c.477T>A (p.Ile159=) n.588T>A n.530+10849T>A | |
| 12 | g.102866614A= | CA2059456986 | PAH | c.491T= (p.Ile164=) c.476T= (p.Ile159=) n.587T= n.530+10848T= | |
| 12 | g.102866614A>C | CA386299516 | PAH | c.491T>G (p.Ile164Ser) c.476T>G (p.Ile159Ser) n.587T>G n.530+10848T>G | |
| 12 | g.102866614A>G | CA229578 | PAH | c.491T>C (p.Ile164Thr) c.476T>C (p.Ile159Thr) n.587T>C n.530+10848T>C | ClinVar dbSNP gnomAD v4 |
| 12 | g.102866614A>T | CA386299517 | PAH | c.491T>A (p.Ile164Asn) c.476T>A (p.Ile159Asn) n.587T>A n.530+10848T>A | |
| 12 | g.102866615T>A | CA386299520 | PAH | c.490A>T (p.Ile164Phe) c.475A>T (p.Ile159Phe) n.586A>T n.530+10847A>T | |
| 12 | g.102866615T>C | CA229576 | PAH | c.490A>G (p.Ile164Val) c.475A>G (p.Ile159Val) n.586A>G n.530+10847A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.102866615T>G | CA386299523 | PAH | c.490A>C (p.Ile164Leu) c.475A>C (p.Ile159Leu) n.586A>C n.530+10847A>C | |
| 12 | g.102866615T= | CA2059456987 | PAH | c.490A= (p.Ile164=) c.475A= (p.Ile159=) n.586A= n.530+10847A= | |
| 12 | g.102866616G>A | CA481332095 | PAH | c.489C>T (p.Asp163=) c.474C>T (p.Asp158=) n.585C>T n.530+10846C>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 12 | g.102866616G>C | CA386299526 | PAH | c.489C>G (p.Asp163Glu) c.474C>G (p.Asp158Glu) n.585C>G n.530+10846C>G | |
| 12 | g.102866616G= | CA2059456988 | PAH | c.489C= (p.Asp163=) c.474C= (p.Asp158=) n.585C= n.530+10846C= | |
| 12 | g.102866616G>T | CA386299528 | PAH | c.489C>A (p.Asp163Glu) c.474C>A (p.Asp158Glu) n.585C>A n.530+10846C>A | dbSNP gnomAD v4 COSMIC |
| 12 | g.102866617T>A | CA386299530 | PAH | c.488A>T (p.Asp163Val) c.473A>T (p.Asp158Val) n.584A>T n.530+10845A>T | |
| 12 | g.102866617T>C | CA386299532 | PAH | c.488A>G (p.Asp163Gly) c.473A>G (p.Asp158Gly) n.584A>G n.530+10845A>G | |
| 12 | g.102866617T>G | CA386299534 | PAH | c.488A>C (p.Asp163Ala) c.473A>C (p.Asp158Ala) n.584A>C n.530+10845A>C | |
| 12 | g.102866618C>A | CA386299539 | PAH | c.487G>T (p.Asp163Tyr) c.472G>T (p.Asp158Tyr) n.583G>T n.530+10844G>T | |
| 12 | g.102866618C>G | CA386299541 | PAH | c.487G>C (p.Asp163His) c.472G>C (p.Asp158His) n.583G>C n.530+10844G>C | |
| 12 | g.102866618C>T | CA386299536 | PAH | c.487G>A (p.Asp163Asn) c.472G>A (p.Asp158Asn) n.583G>A n.530+10844G>A | |
| 12 | g.102866619A>C | CA481332096 | PAH | c.486T>G (p.Ala162=) c.471T>G (p.Ala157=) n.582T>G n.530+10843T>G | |
| 12 | g.102866619A>G | CA481332097 | PAH | c.486T>C (p.Ala162=) c.471T>C (p.Ala157=) n.582T>C n.530+10843T>C | |
| 12 | g.102866619A>T | CA481332098 | PAH | c.486T>A (p.Ala162=) c.471T>A (p.Ala157=) n.582T>A n.530+10843T>A | |
| 12 | g.102866620G>A | CA386299544 | PAH | c.485C>T (p.Ala162Val) c.470C>T (p.Ala157Val) n.581C>T n.530+10842C>T | |
| 12 | g.102866620G>C | CA386299545 | PAH | c.485C>G (p.Ala162Gly) c.470C>G (p.Ala157Gly) n.581C>G n.530+10842C>G | |
| 12 | g.102866620G>T | CA386299548 | PAH | c.485C>A (p.Ala162Asp) c.470C>A (p.Ala157Asp) n.581C>A n.530+10842C>A | |
| 12 | g.102866621C>A | CA6748916 | PAH | c.484G>T (p.Ala162Ser) c.469G>T (p.Ala157Ser) n.580G>T n.530+10841G>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |