Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.94988963A>CCA377677085CYP2C9c.1408A>C (p.Thr470Pro)
c.*417A>C (n.*417A>C)
10g.94988963A>GCA377677086CYP2C9c.1408A>G (p.Thr470Ala)
c.*417A>G (n.*417A>G)
10g.94988963A>TCA377677087CYP2C9c.1408A>T (p.Thr470Ser)
c.*417A>T (n.*417A>T)
10g.94988964C>ACA377677088CYP2C9c.1409C>A (p.Thr470Asn)
c.*418C>A (n.*418C>A)
10g.94988964C=CA1929349770CYP2C9c.1409C= (p.Thr470=)
c.*418C= (n.*418C=)
10g.94988964C>GCA377677089CYP2C9c.1409C>G (p.Thr470Ser)
c.*418C>G (n.*418C>G)
10g.94988964C>TCA5617409CYP2C9c.1409C>T (p.Thr470Ile)
c.*418C>T (n.*418C>T)
dbSNP ExAC gnomAD v2 gnomAD v4
10g.94988965T>ACA470837422CYP2C9c.1410T>A (p.Thr470=)
c.*419T>A (n.*419T>A)
10g.94988965T>CCA5617410CYP2C9c.1410T>C (p.Thr470=)
c.*419T>C (n.*419T>C)
dbSNP ExAC gnomAD v2 gnomAD v4
10g.94988965T>GCA470837423CYP2C9c.1410T>G (p.Thr470=)
c.*419T>G (n.*419T>G)
10g.94988965T=CA1929349776CYP2C9c.1410T= (p.Thr470=)
c.*419T= (n.*419T=)
10g.94988966C>ACA377677090CYP2C9c.1411C>A (p.Pro471Thr)
c.*420C>A (n.*420C>A)
10g.94988966C=CA1929349783CYP2C9c.1411C= (p.Pro471=)
c.*420C= (n.*420C=)
10g.94988966C>GCA377677091CYP2C9c.1411C>G (p.Pro471Ala)
c.*420C>G (n.*420C>G)
dbSNP gnomAD v2 gnomAD v4
10g.94988966C>TCA377677092CYP2C9c.1411C>T (p.Pro471Ser)
c.*420C>T (n.*420C>T)
10g.94988967C>ACA377677093CYP2C9c.1412C>A (p.Pro471Gln)
c.*421C>A (n.*421C>A)
dbSNP
10g.94988967C>GCA377677094CYP2C9c.1412C>G (p.Pro471Arg)
c.*421C>G (n.*421C>G)
10g.94988967C>TCA377677095CYP2C9c.1412C>T (p.Pro471Leu)
c.*421C>T (n.*421C>T)
10g.94988968A=CA1929349786CYP2C9c.1413A= (p.Pro471=)
c.*422A= (n.*422A=)
10g.94988968A>CCA470837424CYP2C9c.1413A>C (p.Pro471=)
c.*422A>C (n.*422A>C)
gnomAD v4
10g.94988968A>GCA470837425CYP2C9c.1413A>G (p.Pro471=)
c.*422A>G (n.*422A>G)
10g.94988968A>TCA5617411CYP2C9c.1413A>T (p.Pro471=)
c.*422A>T (n.*422A>T)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
10g.94988969G>ACA377677096CYP2C9c.1414G>A (p.Val472Ile)
c.*423G>A (n.*423G>A)
10g.94988969G>CCA377677097CYP2C9c.1414G>C (p.Val472Leu)
c.*423G>C (n.*423G>C)
10g.94988969G>TCA377677098CYP2C9c.1414G>T (p.Val472Phe)
c.*423G>T (n.*423G>T)
10g.94988970T>ACA377677099CYP2C9c.1415T>A (p.Val472Asp)
c.*424T>A (n.*424T>A)
10g.94988970T>CCA5617412CYP2C9c.1415T>C (p.Val472Ala)
c.*424T>C (n.*424T>C)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.94988970T>GCA377677100CYP2C9c.1415T>G (p.Val472Gly)
c.*424T>G (n.*424T>G)
10g.94988970T=CA1929349792CYP2C9c.1415T= (p.Val472=)
c.*424T= (n.*424T=)
10g.94988971T>ACA470837426CYP2C9c.1416T>A (p.Val472=)
c.*425T>A (n.*425T>A)
10g.94988971T>CCA470837427CYP2C9c.1416T>C (p.Val472=)
c.*425T>C (n.*425T>C)
10g.94988971T>GCA470837428CYP2C9c.1416T>G (p.Val472=)
c.*425T>G (n.*425T>G)
10g.94988972_94988973dupCA2610266832CYP2C9c.1417_1418dup (p.Asn474SerfsTer?)
c.*426_*427dup (n.*426_*427dup)
gnomAD v4
10g.94988972G>ACA377677101CYP2C9c.1417G>A (p.Val473Ile)
c.*426G>A (n.*426G>A)
10g.94988972G>CCA377677102CYP2C9c.1417G>C (p.Val473Leu)
c.*426G>C (n.*426G>C)
10g.94988972G>TCA377677103CYP2C9c.1417G>T (p.Val473Phe)
c.*426G>T (n.*426G>T)
gnomAD v4
10g.94988973T>ACA377677104CYP2C9c.1418T>A (p.Val473Asp)
c.*427T>A (n.*427T>A)
10g.94988973T>CCA5617413CYP2C9c.1418T>C (p.Val473Ala)
c.*427T>C (n.*427T>C)
dbSNP ExAC gnomAD v2 gnomAD v4
10g.94988973T>GCA377677105CYP2C9c.1418T>G (p.Val473Gly)
c.*427T>G (n.*427T>G)
10g.94988973T=CA1929349795CYP2C9c.1418T= (p.Val473=)
c.*427T= (n.*427T=)
10g.94988974C>ACA470837429CYP2C9c.1419C>A (p.Val473=)
c.*428C>A (n.*428C>A)
10g.94988974C=CA1929349799CYP2C9c.1419C= (p.Val473=)
c.*428C= (n.*428C=)
10g.94988974C>GCA470837430CYP2C9c.1419C>G (p.Val473=)
c.*428C>G (n.*428C>G)
10g.94988974C>TCA211735599CYP2C9c.1419C>T (p.Val473=)
c.*428C>T (n.*428C>T)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.94988975A=CA1929349805CYP2C9c.1420A= (p.Asn474=)
c.*429A= (n.*429A=)
10g.94988975A>CCA377677108CYP2C9c.1420A>C (p.Asn474His)
c.*429A>C (n.*429A>C)
dbSNP
10g.94988975A>GCA377677106CYP2C9c.1420A>G (p.Asn474Asp)
c.*429A>G (n.*429A>G)
10g.94988975A>TCA377677107CYP2C9c.1420A>T (p.Asn474Tyr)
c.*429A>T (n.*429A>T)
10g.94988975_94988976delCA2610266833CYP2C9c.1420_1421del (p.Asn474TrpfsTer?)
c.*429_*430del (n.*429_*430del)
gnomAD v4
10g.94988976A=CA1929349810CYP2C9c.1421A= (p.Asn474=)
c.*430A= (n.*430A=)

Number of alleles fetched