| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.154928607T>A | CA414913568 | F8 | c.5183A>T (p.Tyr1728Phe) c.5078A>T (p.Tyr1693Phe) | |
| X | g.154928607T>C | CA255023 | F8 | c.5183A>G (p.Tyr1728Cys) c.5078A>G (p.Tyr1693Cys) | ClinVar dbSNP |
| X | g.154928607T>G | CA414913571 | F8 | c.5183A>C (p.Tyr1728Ser) c.5078A>C (p.Tyr1693Ser) | |
| X | g.154928607T= | CA2466835743 | F8 | c.5183A= (p.Tyr1728=) c.5078A= (p.Tyr1693=) | |
| X | g.154928608A>C | CA414913573 | F8 | c.5182T>G (p.Tyr1728Asp) c.5077T>G (p.Tyr1693Asp) | |
| X | g.154928608A>G | CA414913575 | F8 | c.5182T>C (p.Tyr1728His) c.5077T>C (p.Tyr1693His) | |
| X | g.154928608A>T | CA414913577 | F8 | c.5182T>A (p.Tyr1728Asn) c.5077T>A (p.Tyr1693Asn) | |
| X | g.154928609A>C | CA414913579 | F8 | c.5181T>G (p.Asp1727Glu) c.5076T>G (p.Asp1692Glu) | |
| X | g.154928609A>G | CA519718346 | F8 | c.5181T>C (p.Asp1727=) c.5076T>C (p.Asp1692=) | |
| X | g.154928609A>T | CA414913584 | F8 | c.5181T>A (p.Asp1727Glu) c.5076T>A (p.Asp1692Glu) | |
| X | g.154928610T>A | CA414913587 | F8 | c.5180A>T (p.Asp1727Val) c.5075A>T (p.Asp1692Val) | |
| X | g.154928610T>C | CA414913592 | F8 | c.5180A>G (p.Asp1727Gly) c.5075A>G (p.Asp1692Gly) | |
| X | g.154928610T>G | CA414913593 | F8 | c.5180A>C (p.Asp1727Ala) c.5075A>C (p.Asp1692Ala) | |
| X | g.154928611C>A | CA414913598 | F8 | c.5179G>T (p.Asp1727Tyr) c.5074G>T (p.Asp1692Tyr) | |
| X | g.154928611C>G | CA414913596 | F8 | c.5179G>C (p.Asp1727His) c.5074G>C (p.Asp1692His) | |
| X | g.154928611C>T | CA414913595 | F8 | c.5179G>A (p.Asp1727Asn) c.5074G>A (p.Asp1692Asn) | |
| X | g.154928612C>A | CA414913600 | F8 | c.5178G>T (p.Trp1726Cys) c.5073G>T (p.Trp1691Cys) | dbSNP |
| X | g.154928612C= | CA2466835744 | F8 | c.5178G= (p.Trp1726=) c.5073G= (p.Trp1691=) | |
| X | g.154928612C>G | CA414913602 | F8 | c.5178G>C (p.Trp1726Cys) c.5073G>C (p.Trp1691Cys) | |
| X | g.154928612C>T | CA414913603 | F8 | c.5178G>A (p.Trp1726Ter) c.5073G>A (p.Trp1691Ter) | |
| X | g.154928613C>A | CA414913604 | F8 | c.5177G>T (p.Trp1726Leu) c.5072G>T (p.Trp1691Leu) | |
| X | g.154928613C>G | CA414913605 | F8 | c.5177G>C (p.Trp1726Ser) c.5072G>C (p.Trp1691Ser) | |
| X | g.154928613C>T | CA414913606 | F8 | c.5177G>A (p.Trp1726Ter) c.5072G>A (p.Trp1691Ter) | |
| X | g.154928614A>C | CA414913608 | F8 | c.5176T>G (p.Trp1726Gly) c.5071T>G (p.Trp1691Gly) | |
| X | g.154928614A>G | CA414913610 | F8 | c.5176T>C (p.Trp1726Arg) c.5071T>C (p.Trp1691Arg) | |
| X | g.154928614A>T | CA414913615 | F8 | c.5176T>A (p.Trp1726Arg) c.5071T>A (p.Trp1691Arg) | |
| X | g.154928615G>A | CA519718349 | F8 | c.5175C>T (p.Leu1725=) c.5070C>T (p.Leu1690=) | |
| X | g.154928615G>C | CA519718348 | F8 | c.5175C>G (p.Leu1725=) c.5070C>G (p.Leu1690=) | |
| X | g.154928615G>T | CA519718347 | F8 | c.5175C>A (p.Leu1725=) c.5070C>A (p.Leu1690=) | gnomAD v4 |
| X | g.154928616A>C | CA414913618 | F8 | c.5174T>G (p.Leu1725Arg) c.5069T>G (p.Leu1690Arg) | |
| X | g.154928616A>G | CA414913620 | F8 | c.5174T>C (p.Leu1725Pro) c.5069T>C (p.Leu1690Pro) | |
| X | g.154928616A>T | CA414913621 | F8 | c.5174T>A (p.Leu1725His) c.5069T>A (p.Leu1690His) | |
| X | g.154928617G>A | CA414913622 | F8 | c.5173C>T (p.Leu1725Phe) c.5068C>T (p.Leu1690Phe) | dbSNP |
| X | g.154928617G>C | CA414913624 | F8 | c.5173C>G (p.Leu1725Val) c.5068C>G (p.Leu1690Val) | |
| X | g.154928617G= | CA2466835745 | F8 | c.5173C= (p.Leu1725=) c.5068C= (p.Leu1690=) | |
| X | g.154928617G>T | CA414913623 | F8 | c.5173C>A (p.Leu1725Ile) c.5068C>A (p.Leu1690Ile) | |
| X | g.154928618C>A | CA414913626 | F8 | c.5172G>T (p.Arg1724Ser) c.5067G>T (p.Arg1689Ser) | |
| X | g.154928618C>G | CA414913627 | F8 | c.5172G>C (p.Arg1724Ser) c.5067G>C (p.Arg1689Ser) | |
| X | g.154928618C>T | CA519718350 | F8 | c.5172G>A (p.Arg1724=) c.5067G>A (p.Arg1689=) | |
| X | g.154928619C>A | CA414913628 | F8 | c.5171G>T (p.Arg1724Met) c.5066G>T (p.Arg1689Met) | |
| X | g.154928619C>G | CA414913631 | F8 | c.5171G>C (p.Arg1724Thr) c.5066G>C (p.Arg1689Thr) | |
| X | g.154928619C>T | CA414913630 | F8 | c.5171G>A (p.Arg1724Lys) c.5066G>A (p.Arg1689Lys) | |
| X | g.154928620T>A | CA414913633 | F8 | c.5170A>T (p.Arg1724Trp) c.5065A>T (p.Arg1689Trp) | |
| X | g.154928620T>C | CA414913635 | F8 | c.5170A>G (p.Arg1724Gly) c.5065A>G (p.Arg1689Gly) | |
| X | g.154928620T>G | CA519718351 | F8 | c.5170A>C (p.Arg1724=) c.5065A>C (p.Arg1689=) | |
| X | g.154928621C>A | CA414913638 | F8 | c.5169G>T (p.Glu1723Asp) c.5064G>T (p.Glu1688Asp) | |
| X | g.154928621C>G | CA414913639 | F8 | c.5169G>C (p.Glu1723Asp) c.5064G>C (p.Glu1688Asp) | |
| X | g.154928621C>T | CA519718352 | F8 | c.5169G>A (p.Glu1723=) c.5064G>A (p.Glu1688=) | gnomAD v4 |
| X | g.154928622T>A | CA414913640 | F8 | c.5168A>T (p.Glu1723Val) c.5063A>T (p.Glu1688Val) | |
| X | g.154928622T>C | CA414913642 | F8 | c.5168A>G (p.Glu1723Gly) c.5063A>G (p.Glu1688Gly) |