Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.94988963A>C | CA377677085 | CYP2C9 | c.1408A>C (p.Thr470Pro) c.*417A>C (n.*417A>C) | |
10 | g.94988963A>G | CA377677086 | CYP2C9 | c.1408A>G (p.Thr470Ala) c.*417A>G (n.*417A>G) | |
10 | g.94988963A>T | CA377677087 | CYP2C9 | c.1408A>T (p.Thr470Ser) c.*417A>T (n.*417A>T) | |
10 | g.94988964C>A | CA377677088 | CYP2C9 | c.1409C>A (p.Thr470Asn) c.*418C>A (n.*418C>A) | |
10 | g.94988964C= | CA1929349770 | CYP2C9 | c.1409C= (p.Thr470=) c.*418C= (n.*418C=) | |
10 | g.94988964C>G | CA377677089 | CYP2C9 | c.1409C>G (p.Thr470Ser) c.*418C>G (n.*418C>G) | |
10 | g.94988964C>T | CA5617409 | CYP2C9 | c.1409C>T (p.Thr470Ile) c.*418C>T (n.*418C>T) | dbSNP ExAC gnomAD v2 gnomAD v4 |
10 | g.94988965T>A | CA470837422 | CYP2C9 | c.1410T>A (p.Thr470=) c.*419T>A (n.*419T>A) | |
10 | g.94988965T>C | CA5617410 | CYP2C9 | c.1410T>C (p.Thr470=) c.*419T>C (n.*419T>C) | dbSNP ExAC gnomAD v2 gnomAD v4 |
10 | g.94988965T>G | CA470837423 | CYP2C9 | c.1410T>G (p.Thr470=) c.*419T>G (n.*419T>G) | |
10 | g.94988965T= | CA1929349776 | CYP2C9 | c.1410T= (p.Thr470=) c.*419T= (n.*419T=) | |
10 | g.94988966C>A | CA377677090 | CYP2C9 | c.1411C>A (p.Pro471Thr) c.*420C>A (n.*420C>A) | |
10 | g.94988966C= | CA1929349783 | CYP2C9 | c.1411C= (p.Pro471=) c.*420C= (n.*420C=) | |
10 | g.94988966C>G | CA377677091 | CYP2C9 | c.1411C>G (p.Pro471Ala) c.*420C>G (n.*420C>G) | dbSNP gnomAD v2 gnomAD v4 |
10 | g.94988966C>T | CA377677092 | CYP2C9 | c.1411C>T (p.Pro471Ser) c.*420C>T (n.*420C>T) | |
10 | g.94988967C>A | CA377677093 | CYP2C9 | c.1412C>A (p.Pro471Gln) c.*421C>A (n.*421C>A) | dbSNP |
10 | g.94988967C>G | CA377677094 | CYP2C9 | c.1412C>G (p.Pro471Arg) c.*421C>G (n.*421C>G) | |
10 | g.94988967C>T | CA377677095 | CYP2C9 | c.1412C>T (p.Pro471Leu) c.*421C>T (n.*421C>T) | |
10 | g.94988968A= | CA1929349786 | CYP2C9 | c.1413A= (p.Pro471=) c.*422A= (n.*422A=) | |
10 | g.94988968A>C | CA470837424 | CYP2C9 | c.1413A>C (p.Pro471=) c.*422A>C (n.*422A>C) | gnomAD v4 |
10 | g.94988968A>G | CA470837425 | CYP2C9 | c.1413A>G (p.Pro471=) c.*422A>G (n.*422A>G) | |
10 | g.94988968A>T | CA5617411 | CYP2C9 | c.1413A>T (p.Pro471=) c.*422A>T (n.*422A>T) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
10 | g.94988969G>A | CA377677096 | CYP2C9 | c.1414G>A (p.Val472Ile) c.*423G>A (n.*423G>A) | |
10 | g.94988969G>C | CA377677097 | CYP2C9 | c.1414G>C (p.Val472Leu) c.*423G>C (n.*423G>C) | |
10 | g.94988969G>T | CA377677098 | CYP2C9 | c.1414G>T (p.Val472Phe) c.*423G>T (n.*423G>T) | |
10 | g.94988970T>A | CA377677099 | CYP2C9 | c.1415T>A (p.Val472Asp) c.*424T>A (n.*424T>A) | |
10 | g.94988970T>C | CA5617412 | CYP2C9 | c.1415T>C (p.Val472Ala) c.*424T>C (n.*424T>C) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.94988970T>G | CA377677100 | CYP2C9 | c.1415T>G (p.Val472Gly) c.*424T>G (n.*424T>G) | |
10 | g.94988970T= | CA1929349792 | CYP2C9 | c.1415T= (p.Val472=) c.*424T= (n.*424T=) | |
10 | g.94988971T>A | CA470837426 | CYP2C9 | c.1416T>A (p.Val472=) c.*425T>A (n.*425T>A) | |
10 | g.94988971T>C | CA470837427 | CYP2C9 | c.1416T>C (p.Val472=) c.*425T>C (n.*425T>C) | |
10 | g.94988971T>G | CA470837428 | CYP2C9 | c.1416T>G (p.Val472=) c.*425T>G (n.*425T>G) | |
10 | g.94988972_94988973dup | CA2610266832 | CYP2C9 | c.1417_1418dup (p.Asn474SerfsTer?) c.*426_*427dup (n.*426_*427dup) | gnomAD v4 |
10 | g.94988972G>A | CA377677101 | CYP2C9 | c.1417G>A (p.Val473Ile) c.*426G>A (n.*426G>A) | |
10 | g.94988972G>C | CA377677102 | CYP2C9 | c.1417G>C (p.Val473Leu) c.*426G>C (n.*426G>C) | |
10 | g.94988972G>T | CA377677103 | CYP2C9 | c.1417G>T (p.Val473Phe) c.*426G>T (n.*426G>T) | gnomAD v4 |
10 | g.94988973T>A | CA377677104 | CYP2C9 | c.1418T>A (p.Val473Asp) c.*427T>A (n.*427T>A) | |
10 | g.94988973T>C | CA5617413 | CYP2C9 | c.1418T>C (p.Val473Ala) c.*427T>C (n.*427T>C) | dbSNP ExAC gnomAD v2 gnomAD v4 |
10 | g.94988973T>G | CA377677105 | CYP2C9 | c.1418T>G (p.Val473Gly) c.*427T>G (n.*427T>G) | |
10 | g.94988973T= | CA1929349795 | CYP2C9 | c.1418T= (p.Val473=) c.*427T= (n.*427T=) | |
10 | g.94988974C>A | CA470837429 | CYP2C9 | c.1419C>A (p.Val473=) c.*428C>A (n.*428C>A) | |
10 | g.94988974C= | CA1929349799 | CYP2C9 | c.1419C= (p.Val473=) c.*428C= (n.*428C=) | |
10 | g.94988974C>G | CA470837430 | CYP2C9 | c.1419C>G (p.Val473=) c.*428C>G (n.*428C>G) | |
10 | g.94988974C>T | CA211735599 | CYP2C9 | c.1419C>T (p.Val473=) c.*428C>T (n.*428C>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.94988975A= | CA1929349805 | CYP2C9 | c.1420A= (p.Asn474=) c.*429A= (n.*429A=) | |
10 | g.94988975A>C | CA377677108 | CYP2C9 | c.1420A>C (p.Asn474His) c.*429A>C (n.*429A>C) | dbSNP |
10 | g.94988975A>G | CA377677106 | CYP2C9 | c.1420A>G (p.Asn474Asp) c.*429A>G (n.*429A>G) | |
10 | g.94988975A>T | CA377677107 | CYP2C9 | c.1420A>T (p.Asn474Tyr) c.*429A>T (n.*429A>T) | |
10 | g.94988975_94988976del | CA2610266833 | CYP2C9 | c.1420_1421del (p.Asn474TrpfsTer?) c.*429_*430del (n.*429_*430del) | gnomAD v4 |
10 | g.94988976A= | CA1929349810 | CYP2C9 | c.1421A= (p.Asn474=) c.*430A= (n.*430A=) |