Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.6174823C>A | CA362662362 | F13A1 | c.1504G>T (p.Gly502Ter) c.1666G>T (p.Gly556Ter) | COSMIC |
6 | g.6174823C= | CA1607969992 | F13A1 | c.1504G= (p.Gly502=) c.1666G= (p.Gly556=) | |
6 | g.6174823C>G | CA362662363 | F13A1 | c.1504G>C (p.Gly502Arg) c.1666G>C (p.Gly556Arg) | |
6 | g.6174823C>T | CA126624 | F13A1 | c.1504G>A (p.Gly502Arg) c.1666G>A (p.Gly556Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.6174824G>A | CA3624324 | F13A1 | c.1503C>T (p.Tyr501=) c.1665C>T (p.Tyr555=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.6174824G>C | CA362662364 | F13A1 | c.1503C>G (p.Tyr501Ter) c.1665C>G (p.Tyr555Ter) | gnomAD v4 |
6 | g.6174824G= | CA1607969993 | F13A1 | c.1503C= (p.Tyr501=) c.1665C= (p.Tyr555=) | |
6 | g.6174824G>T | CA362662365 | F13A1 | c.1503C>A (p.Tyr501Ter) c.1665C>A (p.Tyr555Ter) | ClinVar |
6 | g.6174825T>A | CA362662366 | F13A1 | c.1502A>T (p.Tyr501Phe) c.1664A>T (p.Tyr555Phe) | |
6 | g.6174825T>C | CA362662368 | F13A1 | c.1502A>G (p.Tyr501Cys) c.1664A>G (p.Tyr555Cys) | dbSNP gnomAD v4 |
6 | g.6174825T>G | CA362662367 | F13A1 | c.1502A>C (p.Tyr501Ser) c.1664A>C (p.Tyr555Ser) | |
6 | g.6174825T= | CA1607969994 | F13A1 | c.1502A= (p.Tyr501=) c.1664A= (p.Tyr555=) | |
6 | g.6174826A>C | CA362662369 | F13A1 | c.1501T>G (p.Tyr501Asp) c.1663T>G (p.Tyr555Asp) | |
6 | g.6174826A>G | CA362662370 | F13A1 | c.1501T>C (p.Tyr501His) c.1663T>C (p.Tyr555His) | |
6 | g.6174826A>T | CA362662371 | F13A1 | c.1501T>A (p.Tyr501Asn) c.1663T>A (p.Tyr555Asn) | |
6 | g.6174827C>A | CA362662372 | F13A1 | c.1500G>T (p.Met500Ile) c.1662G>T (p.Met554Ile) | |
6 | g.6174827C= | CA1607969995 | F13A1 | c.1500G= (p.Met500=) c.1662G= (p.Met554=) | |
6 | g.6174827C>G | CA362662373 | F13A1 | c.1500G>C (p.Met500Ile) c.1662G>C (p.Met554Ile) | |
6 | g.6174827C>T | CA3624325 | F13A1 | c.1500G>A (p.Met500Ile) c.1662G>A (p.Met554Ile) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.6174828A= | CA1607969996 | F13A1 | c.1499T= (p.Met500=) c.1661T= (p.Met554=) | |
6 | g.6174828A>C | CA362662374 | F13A1 | c.1499T>G (p.Met500Arg) c.1661T>G (p.Met554Arg) | dbSNP gnomAD v4 |
6 | g.6174828A>G | CA362662375 | F13A1 | c.1499T>C (p.Met500Thr) c.1661T>C (p.Met554Thr) | |
6 | g.6174828A>T | CA362662376 | F13A1 | c.1499T>A (p.Met500Lys) c.1661T>A (p.Met554Lys) | |
6 | g.6174829T>A | CA362662380 | F13A1 | c.1498A>T (p.Met500Leu) c.1660A>T (p.Met554Leu) | |
6 | g.6174829T>C | CA362662381 | F13A1 | c.1498A>G (p.Met500Val) c.1660A>G (p.Met554Val) | gnomAD v4 |
6 | g.6174829T>G | CA362662378 | F13A1 | c.1498A>C (p.Met500Leu) c.1660A>C (p.Met554Leu) | |
6 | g.6174830C>A | CA448499384 | F13A1 | c.1497G>T (p.Leu499=) c.1659G>T (p.Leu553=) | COSMIC |
6 | g.6174830C= | CA1607969997 | F13A1 | c.1497G= (p.Leu499=) c.1659G= (p.Leu553=) | |
6 | g.6174830C>G | CA3624326 | F13A1 | c.1497G>C (p.Leu499=) c.1659G>C (p.Leu553=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.6174830C>T | CA448499385 | F13A1 | c.1497G>A (p.Leu499=) c.1659G>A (p.Leu553=) | |
6 | g.6174831A>C | CA362662386 | F13A1 | c.1496T>G (p.Leu499Arg) c.1658T>G (p.Leu553Arg) | |
6 | g.6174831A>G | CA362662388 | F13A1 | c.1496T>C (p.Leu499Pro) c.1658T>C (p.Leu553Pro) | |
6 | g.6174831A>T | CA362662390 | F13A1 | c.1496T>A (p.Leu499Gln) c.1658T>A (p.Leu553Gln) | |
6 | g.6174832G>A | CA448499387 | F13A1 | c.1495C>T (p.Leu499=) c.1657C>T (p.Leu553=) | |
6 | g.6174832G>C | CA362662393 | F13A1 | c.1495C>G (p.Leu499Val) c.1657C>G (p.Leu553Val) | gnomAD v4 |
6 | g.6174832G>T | CA362662395 | F13A1 | c.1495C>A (p.Leu499Met) c.1657C>A (p.Leu553Met) | |
6 | g.6174833G>A | CA448499388 | F13A1 | c.1494C>T (p.Ala498=) c.1656C>T (p.Ala552=) | gnomAD v4 |
6 | g.6174833G>C | CA448499389 | F13A1 | c.1494C>G (p.Ala498=) c.1656C>G (p.Ala552=) | |
6 | g.6174833G>T | CA448499390 | F13A1 | c.1494C>A (p.Ala498=) c.1656C>A (p.Ala552=) | |
6 | g.6174834G>A | CA133914678 | F13A1 | c.1493C>T (p.Ala498Val) c.1655C>T (p.Ala552Val) | dbSNP |
6 | g.6174834G>C | CA362662397 | F13A1 | c.1493C>G (p.Ala498Gly) c.1655C>G (p.Ala552Gly) | |
6 | g.6174834G= | CA1607969998 | F13A1 | c.1493C= (p.Ala498=) c.1655C= (p.Ala552=) | |
6 | g.6174834G>T | CA362662399 | F13A1 | c.1493C>A (p.Ala498Asp) c.1655C>A (p.Ala552Asp) | |
6 | g.6174835C>A | CA3624327 | F13A1 | c.1492G>T (p.Ala498Ser) c.1654G>T (p.Ala552Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.6174835C= | CA1607969999 | F13A1 | c.1492G= (p.Ala498=) c.1654G= (p.Ala552=) | |
6 | g.6174835C>G | CA362662403 | F13A1 | c.1492G>C (p.Ala498Pro) c.1654G>C (p.Ala552Pro) | |
6 | g.6174835C>T | CA362662404 | F13A1 | c.1492G>A (p.Ala498Thr) c.1654G>A (p.Ala552Thr) | |
6 | g.6174836A>C | CA448499392 | F13A1 | c.1491T>G (p.Thr497=) c.1653T>G (p.Thr551=) | |
6 | g.6174836A>G | CA448499393 | F13A1 | c.1491T>C (p.Thr497=) c.1653T>C (p.Thr551=) | |
6 | g.6174836A>T | CA448499394 | F13A1 | c.1491T>A (p.Thr497=) c.1653T>A (p.Thr551=) |