Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.154928573G>A | CA519374734 | F8 | c.5217C>T (p.Asn1739=) c.5112C>T (p.Asn1704=) | ClinVar dbSNP gnomAD v4 |
X | g.154928573G>C | CA414913431 | F8 | c.5217C>G (p.Asn1739Lys) c.5112C>G (p.Asn1704Lys) | |
X | g.154928573G= | CA2466835730 | F8 | c.5217C= (p.Asn1739=) c.5112C= (p.Asn1704=) | |
X | g.154928573G>T | CA414913433 | F8 | c.5217C>A (p.Asn1739Lys) c.5112C>A (p.Asn1704Lys) | |
X | g.154928574T>A | CA414913435 | F8 | c.5216A>T (p.Asn1739Ile) c.5111A>T (p.Asn1704Ile) | |
X | g.154928574T>C | CA414913436 | F8 | c.5216A>G (p.Asn1739Ser) c.5111A>G (p.Asn1704Ser) | |
X | g.154928574T>G | CA414913438 | F8 | c.5216A>C (p.Asn1739Thr) c.5111A>C (p.Asn1704Thr) | |
X | g.154928576_154928579del | CA2695237880 | F8 | c.5213_5216del (p.Arg1738ThrfsTer?) c.5108_5111del (p.Arg1703ThrfsTer?) | |
X | g.154928575T>A | CA414913440 | F8 | c.5215A>T (p.Asn1739Tyr) c.5110A>T (p.Asn1704Tyr) | |
X | g.154928575T>C | CA414913442 | F8 | c.5215A>G (p.Asn1739Asp) c.5110A>G (p.Asn1704Asp) | |
X | g.154928575T>G | CA414913444 | F8 | c.5215A>C (p.Asn1739His) c.5110A>C (p.Asn1704His) | |
X | g.154928576T>A | CA414913448 | F8 | c.5214A>T (p.Arg1738Ser) c.5109A>T (p.Arg1703Ser) | |
X | g.154928576T>C | CA519374735 | F8 | c.5214A>G (p.Arg1738=) c.5109A>G (p.Arg1703=) | |
X | g.154928576T>G | CA414913447 | F8 | c.5214A>C (p.Arg1738Ser) c.5109A>C (p.Arg1703Ser) | |
X | g.154928577del | CA1139532038 | F8 | c.5213del (p.Arg1738LysfsTer?) c.5108del (p.Arg1703LysfsTer?) | |
X | g.154928577C>A | CA414913450 | F8 | c.5213G>T (p.Arg1738Ile) c.5108G>T (p.Arg1703Ile) | |
X | g.154928577C>G | CA414913452 | F8 | c.5213G>C (p.Arg1738Thr) c.5108G>C (p.Arg1703Thr) | |
X | g.154928577C>T | CA414913454 | F8 | c.5213G>A (p.Arg1738Lys) c.5108G>A (p.Arg1703Lys) | COSMIC COSMIC |
X | g.154928577_154928578delinsCT | CA2466835731 | F8 | c.5212_5213delinsAG (p.Arg1738=) c.5107_5108delinsAG (p.Arg1703=) | |
X | g.154928578T>A | CA414913456 | F8 | c.5212A>T (p.Arg1738Ter) c.5107A>T (p.Arg1703Ter) | |
X | g.154928578T>C | CA414913458 | F8 | c.5212A>G (p.Arg1738Gly) c.5107A>G (p.Arg1703Gly) | |
X | g.154928578T>G | CA519374736 | F8 | c.5212A>C (p.Arg1738=) c.5107A>C (p.Arg1703=) | |
X | g.154928579del | CA2466835732 | F8 | c.5212del (p.Arg1738GlufsTer?) c.5107del (p.Arg1703GlufsTer?) | dbSNP |
X | g.154928579T>A | CA519374737 | F8 | c.5211A>T (p.Leu1737=) c.5106A>T (p.Leu1702=) | |
X | g.154928579T>C | CA519374738 | F8 | c.5211A>G (p.Leu1737=) c.5106A>G (p.Leu1702=) | dbSNP gnomAD v2 gnomAD v4 |
X | g.154928579T>G | CA519374739 | F8 | c.5211A>C (p.Leu1737=) c.5106A>C (p.Leu1702=) | |
X | g.154928579T= | CA2466835733 | F8 | c.5211A= (p.Leu1737=) c.5106A= (p.Leu1702=) | |
X | g.154928580A>C | CA414913460 | F8 | c.5210T>G (p.Leu1737Arg) c.5105T>G (p.Leu1702Arg) | |
X | g.154928580A>G | CA414913462 | F8 | c.5210T>C (p.Leu1737Pro) c.5105T>C (p.Leu1702Pro) | |
X | g.154928580A>T | CA414913464 | F8 | c.5210T>A (p.Leu1737Gln) c.5105T>A (p.Leu1702Gln) | |
X | g.154928581G>A | CA519374740 | F8 | c.5209C>T (p.Leu1737=) c.5104C>T (p.Leu1702=) | COSMIC COSMIC |
X | g.154928581G>C | CA414913466 | F8 | c.5209C>G (p.Leu1737Val) c.5104C>G (p.Leu1702Val) | |
X | g.154928581G>T | CA414913467 | F8 | c.5209C>A (p.Leu1737Ile) c.5104C>A (p.Leu1702Ile) | |
X | g.154928582A>C | CA519374743 | F8 | c.5208T>G (p.Val1736=) c.5103T>G (p.Val1701=) | |
X | g.154928582A>G | CA519374742 | F8 | c.5208T>C (p.Val1736=) c.5103T>C (p.Val1701=) | gnomAD v4 |
X | g.154928582A>T | CA519374741 | F8 | c.5208T>A (p.Val1736=) c.5103T>A (p.Val1701=) | |
X | g.154928583A>C | CA414913471 | F8 | c.5207T>G (p.Val1736Gly) c.5102T>G (p.Val1701Gly) | |
X | g.154928583A>G | CA414913473 | F8 | c.5207T>C (p.Val1736Ala) c.5102T>C (p.Val1701Ala) | |
X | g.154928583A>T | CA414913470 | F8 | c.5207T>A (p.Val1736Asp) c.5102T>A (p.Val1701Asp) | |
X | g.154928584C>A | CA414913475 | F8 | c.5206G>T (p.Val1736Phe) c.5101G>T (p.Val1701Phe) | |
X | g.154928584C= | CA2466835734 | F8 | c.5206G= (p.Val1736=) c.5101G= (p.Val1701=) | |
X | g.154928584C>G | CA414913477 | F8 | c.5206G>C (p.Val1736Leu) c.5101G>C (p.Val1701Leu) | |
X | g.154928584C>T | CA10568027 | F8 | c.5206G>A (p.Val1736Ile) c.5101G>A (p.Val1701Ile) | dbSNP ExAC gnomAD v2 gnomAD v4 |
X | g.154928585A>C | CA414913478 | F8 | c.5205T>G (p.His1735Gln) c.5100T>G (p.His1700Gln) | |
X | g.154928585A>G | CA519374744 | F8 | c.5205T>C (p.His1735=) c.5100T>C (p.His1700=) | gnomAD v4 |
X | g.154928585A>T | CA414913480 | F8 | c.5205T>A (p.His1735Gln) c.5100T>A (p.His1700Gln) | |
X | g.154928586T>A | CA414913482 | F8 | c.5204A>T (p.His1735Leu) c.5099A>T (p.His1700Leu) | |
X | g.154928586T>C | CA414913484 | F8 | c.5204A>G (p.His1735Arg) c.5099A>G (p.His1700Arg) | gnomAD v4 |
X | g.154928586T>G | CA414913486 | F8 | c.5204A>C (p.His1735Pro) c.5099A>C (p.His1700Pro) | |
X | g.154928587G>A | CA414913487 | F8 | c.5203C>T (p.His1735Tyr) c.5098C>T (p.His1700Tyr) |