| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.154957064T>A | CA414911850 | F8 | c.1645A>T (p.Thr549Ser) c.*1521A>T (n.*1521A>T) c.1540A>T (p.Thr514Ser) | |
| X | g.154957064T>C | CA414911851 | F8 | c.1645A>G (p.Thr549Ala) c.*1521A>G (n.*1521A>G) c.1540A>G (p.Thr514Ala) | |
| X | g.154957064T>G | CA414911848 | F8 | c.1645A>C (p.Thr549Pro) c.*1521A>C (n.*1521A>C) c.1540A>C (p.Thr514Pro) | |
| X | g.154957065C>A | CA519358622 | F8 | c.1644G>T (p.Leu548=) c.*1520G>T (n.*1520G>T) c.1539G>T (p.Leu513=) | gnomAD v4 |
| X | g.154957065C>G | CA519358626 | F8 | c.1644G>C (p.Leu548=) c.*1520G>C (n.*1520G>C) c.1539G>C (p.Leu513=) | |
| X | g.154957065C>T | CA519358624 | F8 | c.1644G>A (p.Leu548=) c.*1520G>A (n.*1520G>A) c.1539G>A (p.Leu513=) | |
| X | g.154957066A>C | CA414911852 | F8 | c.1643T>G (p.Leu548Arg) c.*1519T>G (n.*1519T>G) c.1538T>G (p.Leu513Arg) | |
| X | g.154957066A>G | CA16609330 | F8 | c.1643T>C (p.Leu548Pro) c.*1519T>C (n.*1519T>C) c.1538T>C (p.Leu513Pro) | |
| X | g.154957066A>T | CA414911854 | F8 | c.1643T>A (p.Leu548Gln) c.*1519T>A (n.*1519T>A) c.1538T>A (p.Leu513Gln) | |
| X | g.154957067G>A | CA519358632 | F8 | c.1642C>T (p.Leu548=) c.*1518C>T (n.*1518C>T) c.1537C>T (p.Leu513=) | |
| X | g.154957067G>C | CA414911856 | F8 | c.1642C>G (p.Leu548Val) c.*1518C>G (n.*1518C>G) c.1537C>G (p.Leu513Val) | COSMIC COSMIC |
| X | g.154957067G>T | CA414911858 | F8 | c.1642C>A (p.Leu548Met) c.*1518C>A (n.*1518C>A) c.1537C>A (p.Leu513Met) | |
| X | g.154957068G>A | CA519358636 | F8 | c.1641C>T (p.Cys547=) c.*1517C>T (n.*1517C>T) c.1536C>T (p.Cys512=) | |
| X | g.154957068G>C | CA414911863 | F8 | c.1641C>G (p.Cys547Trp) c.*1517C>G (n.*1517C>G) c.1536C>G (p.Cys512Trp) | |
| X | g.154957068G>T | CA414911860 | F8 | c.1641C>A (p.Cys547Ter) c.*1517C>A (n.*1517C>A) c.1536C>A (p.Cys512Ter) | |
| X | g.154957069C>A | CA414911866 | F8 | c.1640G>T (p.Cys547Phe) c.*1516G>T (n.*1516G>T) c.1535G>T (p.Cys512Phe) | dbSNP |
| X | g.154957069C= | CA2466845347 | F8 | c.1640G= (p.Cys547=) c.*1516G= (n.*1516G=) c.1535G= (p.Cys512=) | |
| X | g.154957069C>G | CA414911869 | F8 | c.1640G>C (p.Cys547Ser) c.*1516G>C (n.*1516G>C) c.1535G>C (p.Cys512Ser) | |
| X | g.154957069C>T | CA414911871 | F8 | c.1640G>A (p.Cys547Tyr) c.*1516G>A (n.*1516G>A) c.1535G>A (p.Cys512Tyr) | dbSNP |
| X | g.154957070A= | CA2466845348 | F8 | c.1639T= (p.Cys547=) c.*1515T= (n.*1515T=) c.1534T= (p.Cys512=) | |
| X | g.154957070A>C | CA414911873 | F8 | c.1639T>G (p.Cys547Gly) c.*1515T>G (n.*1515T>G) c.1534T>G (p.Cys512Gly) | |
| X | g.154957070A>G | CA414911874 | F8 | c.1639T>C (p.Cys547Arg) c.*1515T>C (n.*1515T>C) c.1534T>C (p.Cys512Arg) | ClinVar dbSNP |
| X | g.154957070A>T | CA10568426 | F8 | c.1639T>A (p.Cys547Ser) c.*1515T>A (n.*1515T>A) c.1534T>A (p.Cys512Ser) | dbSNP ExAC |
| X | g.154957071C>A | CA519358649 | F8 | c.1638G>T (p.Arg546=) c.*1514G>T (n.*1514G>T) c.1533G>T (p.Arg511=) | |
| X | g.154957071C= | CA2466845349 | F8 | c.1638G= (p.Arg546=) c.*1514G= (n.*1514G=) c.1533G= (p.Arg511=) | |
| X | g.154957071C>G | CA519358650 | F8 | c.1638G>C (p.Arg546=) c.*1514G>C (n.*1514G>C) c.1533G>C (p.Arg511=) | COSMIC COSMIC |
| X | g.154957071C>T | CA519358653 | F8 | c.1638G>A (p.Arg546=) c.*1514G>A (n.*1514G>A) c.1533G>A (p.Arg511=) | dbSNP gnomAD v2 gnomAD v4 |
| X | g.154957072C>A | CA414911876 | F8 | c.1637G>T (p.Arg546Leu) c.*1513G>T (n.*1513G>T) c.1532G>T (p.Arg511Leu) | |
| X | g.154957072C= | CA2466845350 | F8 | c.1637G= (p.Arg546=) c.*1513G= (n.*1513G=) c.1532G= (p.Arg511=) | |
| X | g.154957072C>G | CA414911879 | F8 | c.1637G>C (p.Arg546Pro) c.*1513G>C (n.*1513G>C) c.1532G>C (p.Arg511Pro) | |
| X | g.154957072C>T | CA10568427 | F8 | c.1637G>A (p.Arg546Gln) c.*1513G>A (n.*1513G>A) c.1532G>A (p.Arg511Gln) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| X | g.154957073G>A | CA255112 | F8 | c.1636C>T (p.Arg546Trp) c.*1512C>T (n.*1512C>T) c.1531C>T (p.Arg511Trp) | ClinVar dbSNP gnomAD v4 |
| X | g.154957073G>C | CA414911881 | F8 | c.1636C>G (p.Arg546Gly) c.*1512C>G (n.*1512C>G) c.1531C>G (p.Arg511Gly) | |
| X | g.154957073G= | CA2466845351 | F8 | c.1636C= (p.Arg546=) c.*1512C= (n.*1512C=) c.1531C= (p.Arg511=) | |
| X | g.154957073G>T | CA519358660 | F8 | c.1636C>A (p.Arg546=) c.*1512C>A (n.*1512C>A) c.1531C>A (p.Arg511=) | dbSNP gnomAD v4 |
| X | g.154957074A>C | CA519358665 | F8 | c.1635T>G (p.Pro545=) c.*1511T>G (n.*1511T>G) c.1530T>G (p.Pro510=) | |
| X | g.154957074A>G | CA519358663 | F8 | c.1635T>C (p.Pro545=) c.*1511T>C (n.*1511T>C) c.1530T>C (p.Pro510=) | |
| X | g.154957074A>T | CA519358661 | F8 | c.1635T>A (p.Pro545=) c.*1511T>A (n.*1511T>A) c.1530T>A (p.Pro510=) | COSMIC COSMIC |
| X | g.154957075G>A | CA414911884 | F8 | c.1634C>T (p.Pro545Leu) c.*1510C>T (n.*1510C>T) c.1529C>T (p.Pro510Leu) | |
| X | g.154957075G>C | CA414911889 | F8 | c.1634C>G (p.Pro545Arg) c.*1510C>G (n.*1510C>G) c.1529C>G (p.Pro510Arg) | |
| X | g.154957075G>T | CA414911891 | F8 | c.1634C>A (p.Pro545His) c.*1510C>A (n.*1510C>A) c.1529C>A (p.Pro510His) | |
| X | g.154957076del | CA2695237257 | F8 | c.1634del (p.Pro545LeufsTer4) c.*1510del (n.*1510del) c.1529del (p.Pro510LeufsTer4) | |
| X | g.154957076G>A | CA414911893 | F8 | c.1633C>T (p.Pro545Ser) c.*1509C>T (n.*1509C>T) c.1528C>T (p.Pro510Ser) | |
| X | g.154957076G>C | CA414911894 | F8 | c.1633C>G (p.Pro545Ala) c.*1509C>G (n.*1509C>G) c.1528C>G (p.Pro510Ala) | |
| X | g.154957076G>T | CA414911896 | F8 | c.1633C>A (p.Pro545Thr) c.*1509C>A (n.*1509C>A) c.1528C>A (p.Pro510Thr) | |
| X | g.154957077A>C | CA414911898 | F8 | c.1632T>G (p.Asp544Glu) c.*1508T>G (n.*1508T>G) c.1527T>G (p.Asp509Glu) | |
| X | g.154957077A>G | CA519358672 | F8 | c.1632T>C (p.Asp544=) c.*1508T>C (n.*1508T>C) c.1527T>C (p.Asp509=) | |
| X | g.154957077A>T | CA414911899 | F8 | c.1632T>A (p.Asp544Glu) c.*1508T>A (n.*1508T>A) c.1527T>A (p.Asp509Glu) | |
| X | g.154957077_154957078del | CA2695237258 | F8 | c.1631_1632del (p.Asp544AlafsTer10) c.*1507_*1508del (n.*1507_*1508del) c.1526_1527del (p.Asp509AlafsTer10) | |
| X | g.154957078T>A | CA414911901 | F8 | c.1631A>T (p.Asp544Val) c.*1507A>T (n.*1507A>T) c.1526A>T (p.Asp509Val) | dbSNP |