Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.154928576_154928579del | CA2695237880 | F8 | c.5213_5216del (p.Arg1738ThrfsTer?) c.5108_5111del (p.Arg1703ThrfsTer?) | |
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) | |
X | g.154928587G>C | CA414913489 | F8 | c.5203C>G (p.His1735Asp) c.5098C>G (p.His1700Asp) | |
X | g.154928587G>T | CA414913491 | F8 | c.5203C>A (p.His1735Asn) c.5098C>A (p.His1700Asn) | |
X | g.154928588T>A | CA519374745 | F8 | c.5202A>T (p.Pro1734=) c.5097A>T (p.Pro1699=) | |
X | g.154928588T>C | CA519374747 | F8 | c.5202A>G (p.Pro1734=) c.5097A>G (p.Pro1699=) | |
X | g.154928588T>G | CA519374746 | F8 | c.5202A>C (p.Pro1734=) c.5097A>C (p.Pro1699=) | |
X | g.154928588T= | CA2466835735 | F8 | c.5202A= (p.Pro1734=) c.5097A= (p.Pro1699=) | |
X | g.154928589G>A | CA414913495 | F8 | c.5201C>T (p.Pro1734Leu) c.5096C>T (p.Pro1699Leu) | |
X | g.154928589G>C | CA414913493 | F8 | c.5201C>G (p.Pro1734Arg) c.5096C>G (p.Pro1699Arg) | |
X | g.154928589G= | CA2466835736 | F8 | c.5201C= (p.Pro1734=) c.5096C= (p.Pro1699=) | |
X | g.154928589G>T | CA10568028 | F8 | c.5201C>A (p.Pro1734Gln) c.5096C>A (p.Pro1699Gln) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.154928592dup | CA873340070 | F8 | c.5201dup (p.His1735ThrfsTer25) c.5096dup (p.His1700ThrfsTer25) | dbSNP |
X | g.154928590G>A | CA10568029 | F8 | c.5200C>T (p.Pro1734Ser) c.5095C>T (p.Pro1699Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.154928590G>C | CA414913499 | F8 | c.5200C>G (p.Pro1734Ala) c.5095C>G (p.Pro1699Ala) | |
X | g.154928590G= | CA2466835737 | F8 | c.5200C= (p.Pro1734=) c.5095C= (p.Pro1699=) | |
X | g.154928590G>T | CA414913501 | F8 | c.5200C>A (p.Pro1734Thr) c.5095C>A (p.Pro1699Thr) | |
X | g.154928591G>A | CA519718337 | F8 | c.5199C>T (p.Ser1733=) c.5094C>T (p.Ser1698=) | gnomAD v4 |
X | g.154928591G>C | CA519718338 | F8 | c.5199C>G (p.Ser1733=) c.5094C>G (p.Ser1698=) |