Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.88131178_88131183del | CA2671372363 | ABCG2 | c.410_415del (p.Arg137_Glu138del) | gnomAD v4 |
4 | g.88131179T>A | CA357630451 | ABCG2 | c.413A>T (p.Glu138Val) | |
4 | g.88131179T>C | CA357630452 | ABCG2 | c.413A>G (p.Glu138Gly) | |
4 | g.88131179T>G | CA357630453 | ABCG2 | c.413A>C (p.Glu138Ala) | |
4 | g.88131180C>A | CA357630454 | ABCG2 | c.412G>T (p.Glu138Ter) | COSMIC COSMIC |
4 | g.88131180C= | CA1474616678 | ABCG2 | c.412G= (p.Glu138=) | |
4 | g.88131180C>G | CA357630455 | ABCG2 | c.412G>C (p.Glu138Gln) | COSMIC COSMIC |
4 | g.88131180C>T | CA100893428 | ABCG2 | c.412G>A (p.Glu138Lys) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.88131181T>A | CA357630456 | ABCG2 | c.411A>T (p.Arg137Ser) | |
4 | g.88131181T>C | CA440271069 | ABCG2 | c.411A>G (p.Arg137=) | |
4 | g.88131181T>G | CA357630457 | ABCG2 | c.411A>C (p.Arg137Ser) | |
4 | g.88131182C>A | CA357630458 | ABCG2 | c.410G>T (p.Arg137Ile) | |
4 | g.88131182C= | CA1474616679 | ABCG2 | c.410G= (p.Arg137=) | |
4 | g.88131182C>G | CA3004924 | ABCG2 | c.410G>C (p.Arg137Thr) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.88131182C>T | CA3004923 | ABCG2 | c.410G>A (p.Arg137Lys) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
4 | g.88131183T>A | CA357630460 | ABCG2 | c.409A>T (p.Arg137Ter) | |
4 | g.88131183T>C | CA357630459 | ABCG2 | c.409A>G (p.Arg137Gly) | dbSNP gnomAD v3 gnomAD v4 |
4 | g.88131183T>G | CA440271080 | ABCG2 | c.409A>C (p.Arg137=) | |
4 | g.88131183T= | CA1474616680 | ABCG2 | c.409A= (p.Arg137=) | |
4 | g.88131184C>A | CA440271086 | ABCG2 | c.408G>T (p.Val136=) | |
4 | g.88131184C>G | CA440271085 | ABCG2 | c.408G>C (p.Val136=) | |
4 | g.88131184C>T | CA440271083 | ABCG2 | c.408G>A (p.Val136=) | |
4 | g.88131185A>C | CA357630461 | ABCG2 | c.407T>G (p.Val136Gly) | |
4 | g.88131185A>G | CA357630462 | ABCG2 | c.407T>C (p.Val136Ala) | |
4 | g.88131185A>T | CA357630463 | ABCG2 | c.407T>A (p.Val136Glu) | |
4 | g.88131186C>A | CA357630464 | ABCG2 | c.406G>T (p.Val136Leu) | |
4 | g.88131186C= | CA1474616681 | ABCG2 | c.406G= (p.Val136=) | |
4 | g.88131186C>G | CA357630465 | ABCG2 | c.406G>C (p.Val136Leu) | |
4 | g.88131186C>T | CA3004925 | ABCG2 | c.406G>A (p.Val136Met) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.88131187C>A | CA440271094 | ABCG2 | c.405G>T (p.Thr135=) | |
4 | g.88131187C= | CA1474616682 | ABCG2 | c.405G= (p.Thr135=) | |
4 | g.88131187C>G | CA440271096 | ABCG2 | c.405G>C (p.Thr135=) | |
4 | g.88131187C>T | CA3004926 | ABCG2 | c.405G>A (p.Thr135=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.88131188G>A | CA3004927 | ABCG2 | c.404C>T (p.Thr135Met) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.88131188G>C | CA357630466 | ABCG2 | c.404C>G (p.Thr135Arg) | |
4 | g.88131188G= | CA1474616683 | ABCG2 | c.404C= (p.Thr135=) | |
4 | g.88131188G>T | CA357630467 | ABCG2 | c.404C>A (p.Thr135Lys) | |
4 | g.88131189T>A | CA357630468 | ABCG2 | c.403A>T (p.Thr135Ser) | |
4 | g.88131189T>C | CA357630469 | ABCG2 | c.403A>G (p.Thr135Ala) | |
4 | g.88131189T>G | CA357630470 | ABCG2 | c.403A>C (p.Thr135Pro) | |
4 | g.88131190C>A | CA440271104 | ABCG2 | c.402G>T (p.Leu134=) | |
4 | g.88131190C= | CA1474616684 | ABCG2 | c.402G= (p.Leu134=) | |
4 | g.88131190C>G | CA440271106 | ABCG2 | c.402G>C (p.Leu134=) | |
4 | g.88131190C>T | CA440271112 | ABCG2 | c.402G>A (p.Leu134=) | dbSNP |
4 | g.88131191A= | CA1474616685 | ABCG2 | c.401T= (p.Leu134=) | |
4 | g.88131191A>C | CA357630471 | ABCG2 | c.401T>G (p.Leu134Arg) | dbSNP |
4 | g.88131191A>G | CA357630473 | ABCG2 | c.401T>C (p.Leu134Pro) | |
4 | g.88131191A>T | CA357630472 | ABCG2 | c.401T>A (p.Leu134Gln) | |
4 | g.88131192G>A | CA440271562 | ABCG2 | c.400C>T (p.Leu134=) | |
4 | g.88131192G>C | CA357630474 | ABCG2 | c.400C>G (p.Leu134Val) | dbSNP gnomAD v4 |