| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.87515292_87515310del | CA2578929942 | ABCB1 | c.3206_3224del (p.Val1069GlyfsTer27) n.362_380del n.848_866del n.834_852del c.3014_3032del (p.Val1005GlyfsTer27) c.3416_3434del (p.Val1139GlyfsTer27) | |
| 7 | g.87515302T>A | CA368043818 | ABCB1 | c.3211A>T (p.Ser1071Cys) n.367A>T n.853A>T n.839A>T c.3019A>T (p.Ser1007Cys) c.3421A>T (p.Ser1141Cys) | |
| 7 | g.87515302T>C | CA368043826 | ABCB1 | c.3211A>G (p.Ser1071Gly) n.367A>G n.853A>G n.839A>G c.3019A>G (p.Ser1007Gly) c.3421A>G (p.Ser1141Gly) | |
| 7 | g.87515302T>G | CA368043821 | ABCB1 | c.3211A>C (p.Ser1071Arg) n.367A>C n.853A>C n.839A>C c.3019A>C (p.Ser1007Arg) c.3421A>C (p.Ser1141Arg) | |
| 7 | g.87515303G>A | CA456349360 | ABCB1 | c.3210C>T (p.Gly1070=) n.366C>T n.852C>T n.838C>T c.3018C>T (p.Gly1006=) c.3420C>T (p.Gly1140=) | |
| 7 | g.87515303G>C | CA456349362 | ABCB1 | c.3210C>G (p.Gly1070=) n.366C>G n.852C>G n.838C>G c.3018C>G (p.Gly1006=) c.3420C>G (p.Gly1140=) | |
| 7 | g.87515303G>T | CA456349361 | ABCB1 | c.3210C>A (p.Gly1070=) n.366C>A n.852C>A n.838C>A c.3018C>A (p.Gly1006=) c.3420C>A (p.Gly1140=) | |
| 7 | g.87515304C>A | CA368043828 | ABCB1 | c.3209G>T (p.Gly1070Val) n.365G>T n.851G>T n.837G>T c.3017G>T (p.Gly1006Val) c.3419G>T (p.Gly1140Val) | |
| 7 | g.87515304C>G | CA368043832 | ABCB1 | c.3209G>C (p.Gly1070Ala) n.365G>C n.851G>C n.837G>C c.3017G>C (p.Gly1006Ala) c.3419G>C (p.Gly1140Ala) | |
| 7 | g.87515304C>T | CA368043833 | ABCB1 | c.3209G>A (p.Gly1070Asp) n.365G>A n.851G>A n.837G>A c.3017G>A (p.Gly1006Asp) c.3419G>A (p.Gly1140Asp) | |
| 7 | g.87515305C>A | CA368043837 | ABCB1 | c.3208G>T (p.Gly1070Cys) n.364G>T n.850G>T n.836G>T c.3016G>T (p.Gly1006Cys) c.3418G>T (p.Gly1140Cys) | |
| 7 | g.87515305C>G | CA368043839 | ABCB1 | c.3208G>C (p.Gly1070Arg) n.364G>C n.850G>C n.836G>C c.3016G>C (p.Gly1006Arg) c.3418G>C (p.Gly1140Arg) | |
| 7 | g.87515305C>T | CA368043841 | ABCB1 | c.3208G>A (p.Gly1070Ser) n.364G>A n.850G>A n.836G>A c.3016G>A (p.Gly1006Ser) c.3418G>A (p.Gly1140Ser) | |
| 7 | g.87515306C>A | CA456349366 | ABCB1 | c.3207G>T (p.Val1069=) n.363G>T n.849G>T n.835G>T c.3015G>T (p.Val1005=) c.3417G>T (p.Val1139=) | |
| 7 | g.87515306C= | CA1723626163 | ABCB1 | c.3207G= (p.Val1069=) n.363G= n.849G= n.835G= c.3015G= (p.Val1005=) c.3417G= (p.Val1139=) | |
| 7 | g.87515306C>G | CA456349367 | ABCB1 | c.3207G>C (p.Val1069=) n.363G>C n.849G>C n.835G>C c.3015G>C (p.Val1005=) c.3417G>C (p.Val1139=) | ClinVar dbSNP |
| 7 | g.87515306C>T | CA162101562 | ABCB1 | c.3207G>A (p.Val1069=) n.363G>A n.849G>A n.835G>A c.3015G>A (p.Val1005=) c.3417G>A (p.Val1139=) | dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.87515307A= | CA1723626164 | ABCB1 | c.3206T= (p.Val1069=) n.362T= n.848T= n.834T= c.3014T= (p.Val1005=) c.3416T= (p.Val1139=) | |
| 7 | g.87515307A>C | CA368043847 | ABCB1 | c.3206T>G (p.Val1069Gly) n.362T>G n.848T>G n.834T>G c.3014T>G (p.Val1005Gly) c.3416T>G (p.Val1139Gly) | dbSNP |
| 7 | g.87515307A>G | CA368043849 | ABCB1 | c.3206T>C (p.Val1069Ala) n.362T>C n.848T>C n.834T>C c.3014T>C (p.Val1005Ala) c.3416T>C (p.Val1139Ala) | |
| 7 | g.87515307A>T | CA368043851 | ABCB1 | c.3206T>A (p.Val1069Glu) n.362T>A n.848T>A n.834T>A c.3014T>A (p.Val1005Glu) c.3416T>A (p.Val1139Glu) | |
| 7 | g.87515308C>A | CA368043859 | ABCB1 | c.3205G>T (p.Val1069Leu) n.361G>T n.847G>T n.833G>T c.3013G>T (p.Val1005Leu) c.3415G>T (p.Val1139Leu) | |
| 7 | g.87515308C>G | CA368043854 | ABCB1 | c.3205G>C (p.Val1069Leu) n.361G>C n.847G>C n.833G>C c.3013G>C (p.Val1005Leu) c.3415G>C (p.Val1139Leu) | |
| 7 | g.87515308C>T | CA368043856 | ABCB1 | c.3205G>A (p.Val1069Met) n.361G>A n.847G>A n.833G>A c.3013G>A (p.Val1005Met) c.3415G>A (p.Val1139Met) | |
| 7 | g.87515309C>A | CA456349373 | ABCB1 | c.3204G>T (p.Leu1068=) n.360G>T n.846G>T n.832G>T c.3012G>T (p.Leu1004=) c.3414G>T (p.Leu1138=) | |
| 7 | g.87515309C>G | CA456349376 | ABCB1 | c.3204G>C (p.Leu1068=) n.360G>C n.846G>C n.832G>C c.3012G>C (p.Leu1004=) c.3414G>C (p.Leu1138=) | gnomAD v4 |
| 7 | g.87515309C>T | CA456349374 | ABCB1 | c.3204G>A (p.Leu1068=) n.360G>A n.846G>A n.832G>A c.3012G>A (p.Leu1004=) c.3414G>A (p.Leu1138=) | |
| 7 | g.87515310A>C | CA368043862 | ABCB1 | c.3203T>G (p.Leu1068Arg) n.359T>G n.845T>G n.831T>G c.3011T>G (p.Leu1004Arg) c.3413T>G (p.Leu1138Arg) | |
| 7 | g.87515310A>G | CA368043868 | ABCB1 | c.3203T>C (p.Leu1068Pro) n.359T>C n.845T>C n.831T>C c.3011T>C (p.Leu1004Pro) c.3413T>C (p.Leu1138Pro) | |
| 7 | g.87515310A>T | CA368043865 | ABCB1 | c.3203T>A (p.Leu1068Gln) n.359T>A n.845T>A n.831T>A c.3011T>A (p.Leu1004Gln) c.3413T>A (p.Leu1138Gln) | |
| 7 | g.87515311G>A | CA456349379 | ABCB1 | c.3202C>T (p.Leu1068=) n.358C>T n.844C>T n.830C>T c.3010C>T (p.Leu1004=) c.3412C>T (p.Leu1138=) | |
| 7 | g.87515311G>C | CA4327831 | ABCB1 | c.3202C>G (p.Leu1068Val) n.358C>G n.844C>G n.830C>G c.3010C>G (p.Leu1004Val) c.3412C>G (p.Leu1138Val) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.87515311G= | CA1723626165 | ABCB1 | c.3202C= (p.Leu1068=) n.358C= n.844C= n.830C= c.3010C= (p.Leu1004=) c.3412C= (p.Leu1138=) | |
| 7 | g.87515311G>T | CA368043876 | ABCB1 | c.3202C>A (p.Leu1068Met) n.358C>A n.844C>A n.830C>A c.3010C>A (p.Leu1004Met) c.3412C>A (p.Leu1138Met) | |
| 7 | g.87515312A= | CA1723626166 | ABCB1 | c.3201T= (p.Ala1067=) n.357T= n.843T= n.829T= c.3009T= (p.Ala1003=) c.3411T= (p.Ala1137=) | |
| 7 | g.87515312A>C | CA456349382 | ABCB1 | c.3201T>G (p.Ala1067=) n.357T>G n.843T>G n.829T>G c.3009T>G (p.Ala1003=) c.3411T>G (p.Ala1137=) | ClinVar dbSNP |
| 7 | g.87515312A>G | CA456349384 | ABCB1 | c.3201T>C (p.Ala1067=) n.357T>C n.843T>C n.829T>C c.3009T>C (p.Ala1003=) c.3411T>C (p.Ala1137=) | |
| 7 | g.87515312A>T | CA456349383 | ABCB1 | c.3201T>A (p.Ala1067=) n.357T>A n.843T>A n.829T>A c.3009T>A (p.Ala1003=) c.3411T>A (p.Ala1137=) | |
| 7 | g.87515313G>A | CA4327832 | ABCB1 | c.3200C>T (p.Ala1067Val) n.356C>T n.842C>T n.828C>T c.3008C>T (p.Ala1003Val) c.3410C>T (p.Ala1137Val) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.87515313G>C | CA368043881 | ABCB1 | c.3200C>G (p.Ala1067Gly) n.356C>G n.842C>G n.828C>G c.3008C>G (p.Ala1003Gly) c.3410C>G (p.Ala1137Gly) | |
| 7 | g.87515313G= | CA1723626167 | ABCB1 | c.3200C= (p.Ala1067=) n.356C= n.842C= n.828C= c.3008C= (p.Ala1003=) c.3410C= (p.Ala1137=) | |
| 7 | g.87515313G>T | CA162101563 | ABCB1 | c.3200C>A (p.Ala1067Asp) n.356C>A n.842C>A n.828C>A c.3008C>A (p.Ala1003Asp) c.3410C>A (p.Ala1137Asp) | dbSNP |
| 7 | g.87515314C>A | CA368043890 | ABCB1 | c.3199G>T (p.Ala1067Ser) n.355G>T n.841G>T n.827G>T c.3007G>T (p.Ala1003Ser) c.3409G>T (p.Ala1137Ser) | |
| 7 | g.87515314C= | CA1723626168 | ABCB1 | c.3199G= (p.Ala1067=) n.355G= n.841G= n.827G= c.3007G= (p.Ala1003=) c.3409G= (p.Ala1137=) | |
| 7 | g.87515314C>G | CA368043888 | ABCB1 | c.3199G>C (p.Ala1067Pro) n.355G>C n.841G>C n.827G>C c.3007G>C (p.Ala1003Pro) c.3409G>C (p.Ala1137Pro) | gnomAD v4 |
| 7 | g.87515314C>T | CA4327833 | ABCB1 | c.3199G>A (p.Ala1067Thr) n.355G>A n.841G>A n.827G>A c.3007G>A (p.Ala1003Thr) c.3409G>A (p.Ala1137Thr) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.87515315C>A | CA456349388 | ABCB1 | c.3198G>T (p.Leu1066=) n.354G>T n.840G>T n.826G>T c.3006G>T (p.Leu1002=) c.3408G>T (p.Leu1136=) | |
| 7 | g.87515315C>G | CA456349387 | ABCB1 | c.3198G>C (p.Leu1066=) n.354G>C n.840G>C n.826G>C c.3006G>C (p.Leu1002=) c.3408G>C (p.Leu1136=) | |
| 7 | g.87515315C>T | CA456349386 | ABCB1 | c.3198G>A (p.Leu1066=) n.354G>A n.840G>A n.826G>A c.3006G>A (p.Leu1002=) c.3408G>A (p.Leu1136=) | |
| 7 | g.87515316A= | CA1723626169 | ABCB1 | c.3197T= (p.Leu1066=) n.353T= n.839T= n.825T= c.3005T= (p.Leu1002=) c.3407T= (p.Leu1136=) | |
| 7 | g.87515316A>C | CA368043894 | ABCB1 | c.3197T>G (p.Leu1066Arg) n.353T>G n.839T>G n.825T>G c.3005T>G (p.Leu1002Arg) c.3407T>G (p.Leu1136Arg) | |
| 7 | g.87515316A>G | CA162101565 | ABCB1 | c.3197T>C (p.Leu1066Pro) n.353T>C n.839T>C n.825T>C c.3005T>C (p.Leu1002Pro) c.3407T>C (p.Leu1136Pro) | dbSNP |
| 7 | g.87515316A>T | CA368043903 | ABCB1 | c.3197T>A (p.Leu1066Gln) n.353T>A n.839T>A n.825T>A c.3005T>A (p.Leu1002Gln) c.3407T>A (p.Leu1136Gln) | gnomAD v4 |
| 7 | g.87515317G>A | CA456349391 | ABCB1 | c.3196C>T (p.Leu1066=) n.352C>T n.838C>T n.824C>T c.3004C>T (p.Leu1002=) c.3406C>T (p.Leu1136=) | gnomAD v4 |
| 7 | g.87515317G>C | CA368043906 | ABCB1 | c.3196C>G (p.Leu1066Val) n.352C>G n.838C>G n.824C>G c.3004C>G (p.Leu1002Val) c.3406C>G (p.Leu1136Val) | |
| 7 | g.87515317G>T | CA368043910 | ABCB1 | c.3196C>A (p.Leu1066Met) n.352C>A n.838C>A n.824C>A c.3004C>A (p.Leu1002Met) c.3406C>A (p.Leu1136Met) | gnomAD v4 |
| 7 | g.87515318C>A | CA456349392 | ABCB1 | c.3195G>T (p.Thr1065=) n.351G>T n.837G>T n.823G>T c.3003G>T (p.Thr1001=) c.3405G>T (p.Thr1135=) | |
| 7 | g.87515318C= | CA1723626170 | ABCB1 | c.3195G= (p.Thr1065=) n.351G= n.837G= n.823G= c.3003G= (p.Thr1001=) c.3405G= (p.Thr1135=) | |
| 7 | g.87515318C>G | CA456349396 | ABCB1 | c.3195G>C (p.Thr1065=) n.351G>C n.837G>C n.823G>C c.3003G>C (p.Thr1001=) c.3405G>C (p.Thr1135=) | |
| 7 | g.87515318C>T | CA4327834 | ABCB1 | c.3195G>A (p.Thr1065=) n.351G>A n.837G>A n.823G>A c.3003G>A (p.Thr1001=) c.3405G>A (p.Thr1135=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.87515319G>A | CA4327835 | ABCB1 | c.3194C>T (p.Thr1065Met) n.350C>T n.836C>T n.822C>T c.3002C>T (p.Thr1001Met) c.3404C>T (p.Thr1135Met) | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
| 7 | g.87515319G>C | CA368043936 | ABCB1 | c.3194C>G (p.Thr1065Arg) n.350C>G n.836C>G n.822C>G c.3002C>G (p.Thr1001Arg) c.3404C>G (p.Thr1135Arg) | |
| 7 | g.87515319G= | CA1723626171 | ABCB1 | c.3194C= (p.Thr1065=) n.350C= n.836C= n.822C= c.3002C= (p.Thr1001=) c.3404C= (p.Thr1135=) | |
| 7 | g.87515319G>T | CA368043930 | ABCB1 | c.3194C>A (p.Thr1065Lys) n.350C>A n.836C>A n.822C>A c.3002C>A (p.Thr1001Lys) c.3404C>A (p.Thr1135Lys) | gnomAD v4 |
| 7 | g.87515320T>A | CA368043940 | ABCB1 | c.3193A>T (p.Thr1065Ser) n.349A>T n.835A>T n.821A>T c.3001A>T (p.Thr1001Ser) c.3403A>T (p.Thr1135Ser) | |
| 7 | g.87515320T>C | CA368043942 | ABCB1 | c.3193A>G (p.Thr1065Ala) n.349A>G n.835A>G n.821A>G c.3001A>G (p.Thr1001Ala) c.3403A>G (p.Thr1135Ala) | |
| 7 | g.87515320T>G | CA368043946 | ABCB1 | c.3193A>C (p.Thr1065Pro) n.349A>C n.835A>C n.821A>C c.3001A>C (p.Thr1001Pro) c.3403A>C (p.Thr1135Pro) | |
| 7 | g.87515321C>A | CA368043951 | ABCB1 | c.3192G>T (p.Gln1064His) n.348G>T n.834G>T n.820G>T c.3000G>T (p.Gln1000His) c.3402G>T (p.Gln1134His) | |
| 7 | g.87515321C>G | CA368043956 | ABCB1 | c.3192G>C (p.Gln1064His) n.348G>C n.834G>C n.820G>C c.3000G>C (p.Gln1000His) c.3402G>C (p.Gln1134His) | |
| 7 | g.87515321C>T | CA456349403 | ABCB1 | c.3192G>A (p.Gln1064=) n.348G>A n.834G>A n.820G>A c.3000G>A (p.Gln1000=) c.3402G>A (p.Gln1134=) | gnomAD v4 |
| 7 | g.87515322T>A | CA368043960 | ABCB1 | c.3191A>T (p.Gln1064Leu) n.347A>T n.833A>T n.819A>T c.2999A>T (p.Gln1000Leu) c.3401A>T (p.Gln1134Leu) | |
| 7 | g.87515322T>C | CA368043963 | ABCB1 | c.3191A>G (p.Gln1064Arg) n.347A>G n.833A>G n.819A>G c.2999A>G (p.Gln1000Arg) c.3401A>G (p.Gln1134Arg) | |
| 7 | g.87515322T>G | CA368043967 | ABCB1 | c.3191A>C (p.Gln1064Pro) n.347A>C n.833A>C n.819A>C c.2999A>C (p.Gln1000Pro) c.3401A>C (p.Gln1134Pro) | |
| 7 | g.87515323G>A | CA368043968 | ABCB1 | c.3190C>T (p.Gln1064Ter) n.346C>T n.832C>T n.818C>T c.2998C>T (p.Gln1000Ter) c.3400C>T (p.Gln1134Ter) | |
| 7 | g.87515323G>C | CA368043969 | ABCB1 | c.3190C>G (p.Gln1064Glu) n.346C>G n.832C>G n.818C>G c.2998C>G (p.Gln1000Glu) c.3400C>G (p.Gln1134Glu) | |
| 7 | g.87515323G>T | CA368043972 | ABCB1 | c.3190C>A (p.Gln1064Lys) n.346C>A n.832C>A n.818C>A c.2998C>A (p.Gln1000Lys) c.3400C>A (p.Gln1134Lys) | |
| 7 | g.87515324G>A | CA456349404 | ABCB1 | c.3189C>T (p.Gly1063=) n.345C>T n.831C>T n.817C>T c.2997C>T (p.Gly999=) c.3399C>T (p.Gly1133=) | |
| 7 | g.87515324G>C | CA162101570 | ABCB1 | c.3189C>G (p.Gly1063=) n.345C>G n.831C>G n.817C>G c.2997C>G (p.Gly999=) c.3399C>G (p.Gly1133=) | dbSNP |
| 7 | g.87515324G= | CA1723626172 | ABCB1 | c.3189C= (p.Gly1063=) n.345C= n.831C= n.817C= c.2997C= (p.Gly999=) c.3399C= (p.Gly1133=) | |
| 7 | g.87515324G>T | CA456349408 | ABCB1 | c.3189C>A (p.Gly1063=) n.345C>A n.831C>A n.817C>A c.2997C>A (p.Gly999=) c.3399C>A (p.Gly1133=) | |
| 7 | g.87515325C>A | CA368043988 | ABCB1 | c.3188G>T (p.Gly1063Val) n.344G>T n.830G>T n.816G>T c.2996G>T (p.Gly999Val) c.3398G>T (p.Gly1133Val) | |
| 7 | g.87515325C= | CA1723626173 | ABCB1 | c.3188G= (p.Gly1063=) n.344G= n.830G= n.816G= c.2996G= (p.Gly999=) c.3398G= (p.Gly1133=) | |
| 7 | g.87515325C>G | CA162101572 | ABCB1 | c.3188G>C (p.Gly1063Ala) n.344G>C n.830G>C n.816G>C c.2996G>C (p.Gly999Ala) c.3398G>C (p.Gly1133Ala) | dbSNP |
| 7 | g.87515325C>T | CA368043982 | ABCB1 | c.3188G>A (p.Gly1063Asp) n.344G>A n.830G>A n.816G>A c.2996G>A (p.Gly999Asp) c.3398G>A (p.Gly1133Asp) | dbSNP |
| 7 | g.87515327del | CA2683605177 | ABCB1 | c.3188del (p.Gly1063AlafsTer?) n.344del n.830del n.816del c.2996del (p.Gly999AlafsTer?) c.3398del (p.Gly1133AlafsTer?) | gnomAD v4 |
| 7 | g.87515326C>A | CA4327836 | ABCB1 | c.3187G>T (p.Gly1063Cys) n.343G>T n.829G>T n.815G>T c.2995G>T (p.Gly999Cys) c.3397G>T (p.Gly1133Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.87515326C= | CA1723626174 | ABCB1 | c.3187G= (p.Gly1063=) n.343G= n.829G= n.815G= c.2995G= (p.Gly999=) c.3397G= (p.Gly1133=) | |
| 7 | g.87515326C>G | CA368043999 | ABCB1 | c.3187G>C (p.Gly1063Arg) n.343G>C n.829G>C n.815G>C c.2995G>C (p.Gly999Arg) c.3397G>C (p.Gly1133Arg) | |
| 7 | g.87515326C>T | CA368044006 | ABCB1 | c.3187G>A (p.Gly1063Ser) n.343G>A n.829G>A n.815G>A c.2995G>A (p.Gly999Ser) c.3397G>A (p.Gly1133Ser) | gnomAD v4 |
| 7 | g.87515327C>A | CA368044009 | ABCB1 | c.3186G>T (p.Lys1062Asn) n.342G>T n.828G>T n.814G>T c.2994G>T (p.Lys998Asn) c.3396G>T (p.Lys1132Asn) | dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.87515327C= | CA1723626175 | ABCB1 | c.3186G= (p.Lys1062=) n.342G= n.828G= n.814G= c.2994G= (p.Lys998=) c.3396G= (p.Lys1132=) | |
| 7 | g.87515327C>G | CA368044013 | ABCB1 | c.3186G>C (p.Lys1062Asn) n.342G>C n.828G>C n.814G>C c.2994G>C (p.Lys998Asn) c.3396G>C (p.Lys1132Asn) | |
| 7 | g.87515327C>T | CA456349414 | ABCB1 | c.3186G>A (p.Lys1062=) n.342G>A n.828G>A n.814G>A c.2994G>A (p.Lys998=) c.3396G>A (p.Lys1132=) | |
| 7 | g.87515328T>A | CA368044018 | ABCB1 | c.3185A>T (p.Lys1062Met) n.341A>T n.827A>T n.813A>T c.2993A>T (p.Lys998Met) c.3395A>T (p.Lys1132Met) | |
| 7 | g.87515328T>C | CA368044016 | ABCB1 | c.3185A>G (p.Lys1062Arg) n.341A>G n.827A>G n.813A>G c.2993A>G (p.Lys998Arg) c.3395A>G (p.Lys1132Arg) | ClinVar dbSNP |
| 7 | g.87515328T>G | CA368044017 | ABCB1 | c.3185A>C (p.Lys1062Thr) n.341A>C n.827A>C n.813A>C c.2993A>C (p.Lys998Thr) c.3395A>C (p.Lys1132Thr) | |
| 7 | g.87515328T= | CA1723626176 | ABCB1 | c.3185A= (p.Lys1062=) n.341A= n.827A= n.813A= c.2993A= (p.Lys998=) c.3395A= (p.Lys1132=) | |
| 7 | g.87515329T>A | CA368044021 | ABCB1 | c.3184A>T (p.Lys1062Ter) n.340A>T n.826A>T n.812A>T c.2992A>T (p.Lys998Ter) c.3394A>T (p.Lys1132Ter) | |
| 7 | g.87515329T>C | CA368044028 | ABCB1 | c.3184A>G (p.Lys1062Glu) n.340A>G n.826A>G n.812A>G c.2992A>G (p.Lys998Glu) c.3394A>G (p.Lys1132Glu) | |
| 7 | g.87515329T>G | CA368044031 | ABCB1 | c.3184A>C (p.Lys1062Gln) n.340A>C n.826A>C n.812A>C c.2992A>C (p.Lys998Gln) c.3394A>C (p.Lys1132Gln) | |
| 7 | g.87515330C>A | CA368044040 | ABCB1 | c.3183G>T (p.Lys1061Asn) n.339G>T n.825G>T n.811G>T c.2991G>T (p.Lys997Asn) c.3393G>T (p.Lys1131Asn) | dbSNP gnomAD v4 |
| 7 | g.87515330C= | CA1723626177 | ABCB1 | c.3183G= (p.Lys1061=) n.339G= n.825G= n.811G= c.2991G= (p.Lys997=) c.3393G= (p.Lys1131=) | |
| 7 | g.87515330C>G | CA368044044 | ABCB1 | c.3183G>C (p.Lys1061Asn) n.339G>C n.825G>C n.811G>C c.2991G>C (p.Lys997Asn) c.3393G>C (p.Lys1131Asn) | |
| 7 | g.87515330C>T | CA456349419 | ABCB1 | c.3183G>A (p.Lys1061=) n.339G>A n.825G>A n.811G>A c.2991G>A (p.Lys997=) c.3393G>A (p.Lys1131=) | |
| 7 | g.87515331T>A | CA368044045 | ABCB1 | c.3182A>T (p.Lys1061Met) n.338A>T n.824A>T n.810A>T c.2990A>T (p.Lys997Met) c.3392A>T (p.Lys1131Met) | |
| 7 | g.87515331T>C | CA368044047 | ABCB1 | c.3182A>G (p.Lys1061Arg) n.338A>G n.824A>G n.810A>G c.2990A>G (p.Lys997Arg) c.3392A>G (p.Lys1131Arg) | dbSNP gnomAD v3 gnomAD v4 COSMIC |
| 7 | g.87515331T>G | CA368044046 | ABCB1 | c.3182A>C (p.Lys1061Thr) n.338A>C n.824A>C n.810A>C c.2990A>C (p.Lys997Thr) c.3392A>C (p.Lys1131Thr) | COSMIC |
| 7 | g.87515331T= | CA1723626178 | ABCB1 | c.3182A= (p.Lys1061=) n.338A= n.824A= n.810A= c.2990A= (p.Lys997=) c.3392A= (p.Lys1131=) | |
| 7 | g.87515332T>A | CA368044051 | ABCB1 | c.3181A>T (p.Lys1061Ter) n.337A>T n.823A>T n.809A>T c.2989A>T (p.Lys997Ter) c.3391A>T (p.Lys1131Ter) | |
| 7 | g.87515332T>C | CA368044055 | ABCB1 | c.3181A>G (p.Lys1061Glu) n.337A>G n.823A>G n.809A>G c.2989A>G (p.Lys997Glu) c.3391A>G (p.Lys1131Glu) | |
| 7 | g.87515332T>G | CA368044056 | ABCB1 | c.3181A>C (p.Lys1061Gln) n.337A>C n.823A>C n.809A>C c.2989A>C (p.Lys997Gln) c.3391A>C (p.Lys1131Gln) | |
| 7 | g.87515333C>A | CA456349426 | ABCB1 | c.3180G>T (p.Val1060=) n.336G>T n.822G>T n.808G>T c.2988G>T (p.Val996=) c.3390G>T (p.Val1130=) | dbSNP |
| 7 | g.87515333C= | CA1723626179 | ABCB1 | c.3180G= (p.Val1060=) n.336G= n.822G= n.808G= c.2988G= (p.Val996=) c.3390G= (p.Val1130=) | |
| 7 | g.87515333C>G | CA456349427 | ABCB1 | c.3180G>C (p.Val1060=) n.336G>C n.822G>C n.808G>C c.2988G>C (p.Val996=) c.3390G>C (p.Val1130=) | |
| 7 | g.87515333C>T | CA162101577 | ABCB1 | c.3180G>A (p.Val1060=) n.336G>A n.822G>A n.808G>A c.2988G>A (p.Val996=) c.3390G>A (p.Val1130=) | dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.87515334A>C | CA368044057 | ABCB1 | c.3179T>G (p.Val1060Gly) n.335T>G n.821T>G n.807T>G c.2987T>G (p.Val996Gly) c.3389T>G (p.Val1130Gly) | |
| 7 | g.87515334A>G | CA368044059 | ABCB1 | c.3179T>C (p.Val1060Ala) n.335T>C n.821T>C n.807T>C c.2987T>C (p.Val996Ala) c.3389T>C (p.Val1130Ala) | |
| 7 | g.87515334A>T | CA368044066 | ABCB1 | c.3179T>A (p.Val1060Glu) n.335T>A n.821T>A n.807T>A c.2987T>A (p.Val996Glu) c.3389T>A (p.Val1130Glu) | |
| 7 | g.87515335C>A | CA368044070 | ABCB1 | c.3178G>T (p.Val1060Leu) n.334G>T n.820G>T n.806G>T c.2986G>T (p.Val996Leu) c.3388G>T (p.Val1130Leu) | |
| 7 | g.87515335C= | CA1723626180 | ABCB1 | c.3178G= (p.Val1060=) n.334G= n.820G= n.806G= c.2986G= (p.Val996=) c.3388G= (p.Val1130=) | |
| 7 | g.87515335C>G | CA368044071 | ABCB1 | c.3178G>C (p.Val1060Leu) n.334G>C n.820G>C n.806G>C c.2986G>C (p.Val996Leu) c.3388G>C (p.Val1130Leu) | |
| 7 | g.87515335C>T | CA368044072 | ABCB1 | c.3178G>A (p.Val1060Met) n.334G>A n.820G>A n.806G>A c.2986G>A (p.Val996Met) c.3388G>A (p.Val1130Met) | ClinVar dbSNP gnomAD v4 |
| 7 | g.87515336C>A | CA368044074 | ABCB1 | c.3177G>T (p.Glu1059Asp) n.333G>T n.819G>T n.805G>T c.2985G>T (p.Glu995Asp) c.3387G>T (p.Glu1129Asp) | |
| 7 | g.87515336C>G | CA368044077 | ABCB1 | c.3177G>C (p.Glu1059Asp) n.333G>C n.819G>C n.805G>C c.2985G>C (p.Glu995Asp) c.3387G>C (p.Glu1129Asp) | |
| 7 | g.87515336C>T | CA456349435 | ABCB1 | c.3177G>A (p.Glu1059=) n.333G>A n.819G>A n.805G>A c.2985G>A (p.Glu995=) c.3387G>A (p.Glu1129=) | dbSNP COSMIC |
| 7 | g.87515337T>A | CA368044083 | ABCB1 | c.3176A>T (p.Glu1059Val) n.332A>T n.818A>T n.804A>T c.2984A>T (p.Glu995Val) c.3386A>T (p.Glu1129Val) | |
| 7 | g.87515337T>C | CA368044094 | ABCB1 | c.3176A>G (p.Glu1059Gly) n.332A>G n.818A>G n.804A>G c.2984A>G (p.Glu995Gly) c.3386A>G (p.Glu1129Gly) | |
| 7 | g.87515337T>G | CA368044089 | ABCB1 | c.3176A>C (p.Glu1059Ala) n.332A>C n.818A>C n.804A>C c.2984A>C (p.Glu995Ala) c.3386A>C (p.Glu1129Ala) | |
| 7 | g.87515338C>A | CA368044098 | ABCB1 | c.3175G>T (p.Glu1059Ter) n.331G>T n.817G>T n.803G>T c.2983G>T (p.Glu995Ter) c.3385G>T (p.Glu1129Ter) | dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.87515338C= | CA1723626181 | ABCB1 | c.3175G= (p.Glu1059=) n.331G= n.817G= n.803G= c.2983G= (p.Glu995=) c.3385G= (p.Glu1129=) | |
| 7 | g.87515338C>G | CA368044100 | ABCB1 | c.3175G>C (p.Glu1059Gln) n.331G>C n.817G>C n.803G>C c.2983G>C (p.Glu995Gln) c.3385G>C (p.Glu1129Gln) | |
| 7 | g.87515338C>T | CA368044103 | ABCB1 | c.3175G>A (p.Glu1059Lys) n.331G>A n.817G>A n.803G>A c.2983G>A (p.Glu995Lys) c.3385G>A (p.Glu1129Lys) | |
| 7 | g.87515339C>A | CA456349441 | ABCB1 | c.3174G>T (p.Leu1058=) n.330G>T n.816G>T n.802G>T c.2982G>T (p.Leu994=) c.3384G>T (p.Leu1128=) | |
| 7 | g.87515339C>G | CA456349443 | ABCB1 | c.3174G>C (p.Leu1058=) n.330G>C n.816G>C n.802G>C c.2982G>C (p.Leu994=) c.3384G>C (p.Leu1128=) | |
| 7 | g.87515339C>T | CA456349442 | ABCB1 | c.3174G>A (p.Leu1058=) n.330G>A n.816G>A n.802G>A c.2982G>A (p.Leu994=) c.3384G>A (p.Leu1128=) | gnomAD v4 |
| 7 | g.87515340A>C | CA368044107 | ABCB1 | c.3173T>G (p.Leu1058Arg) n.329T>G n.815T>G n.801T>G c.2981T>G (p.Leu994Arg) c.3383T>G (p.Leu1128Arg) | |
| 7 | g.87515340A>G | CA368044112 | ABCB1 | c.3173T>C (p.Leu1058Pro) n.329T>C n.815T>C n.801T>C c.2981T>C (p.Leu994Pro) c.3383T>C (p.Leu1128Pro) | |
| 7 | g.87515340A>T | CA368044117 | ABCB1 | c.3173T>A (p.Leu1058Gln) n.329T>A n.815T>A n.801T>A c.2981T>A (p.Leu994Gln) c.3383T>A (p.Leu1128Gln) | |
| 7 | g.87515341G>A | CA456349447 | ABCB1 | c.3172C>T (p.Leu1058=) n.328C>T n.814C>T n.800C>T c.2980C>T (p.Leu994=) c.3382C>T (p.Leu1128=) | |
| 7 | g.87515341G>C | CA368044121 | ABCB1 | c.3172C>G (p.Leu1058Val) n.328C>G n.814C>G n.800C>G c.2980C>G (p.Leu994Val) c.3382C>G (p.Leu1128Val) | dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.87515341G= | CA1723626182 | ABCB1 | c.3172C= (p.Leu1058=) n.328C= n.814C= n.800C= c.2980C= (p.Leu994=) c.3382C= (p.Leu1128=) | |
| 7 | g.87515341G>T | CA368044122 | ABCB1 | c.3172C>A (p.Leu1058Met) n.328C>A n.814C>A n.800C>A c.2980C>A (p.Leu994Met) c.3382C>A (p.Leu1128Met) | |
| 7 | g.87515342G>A | CA456349451 | ABCB1 | c.3171C>T (p.Ser1057=) n.327C>T n.813C>T n.799C>T c.2979C>T (p.Ser993=) c.3381C>T (p.Ser1127=) | |
| 7 | g.87515342G>C | CA368044123 | ABCB1 | c.3171C>G (p.Ser1057Arg) n.327C>G n.813C>G n.799C>G c.2979C>G (p.Ser993Arg) c.3381C>G (p.Ser1127Arg) | |
| 7 | g.87515342G= | CA1723626183 | ABCB1 | c.3171C= (p.Ser1057=) n.327C= n.813C= n.799C= c.2979C= (p.Ser993=) c.3381C= (p.Ser1127=) | |
| 7 | g.87515342G>T | CA4327837 | ABCB1 | c.3171C>A (p.Ser1057Arg) n.327C>A n.813C>A n.799C>A c.2979C>A (p.Ser993Arg) c.3381C>A (p.Ser1127Arg) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.87515343C>A | CA368044130 | ABCB1 | c.3170G>T (p.Ser1057Ile) n.326G>T n.812G>T n.798G>T c.2978G>T (p.Ser993Ile) c.3380G>T (p.Ser1127Ile) | |
| 7 | g.87515343C= | CA1723626184 | ABCB1 | c.3170G= (p.Ser1057=) n.326G= n.812G= n.798G= c.2978G= (p.Ser993=) c.3380G= (p.Ser1127=) | |
| 7 | g.87515343C>G | CA368044135 | ABCB1 | c.3170G>C (p.Ser1057Thr) n.326G>C n.812G>C n.798G>C c.2978G>C (p.Ser993Thr) c.3380G>C (p.Ser1127Thr) | |
| 7 | g.87515343C>T | CA368044146 | ABCB1 | c.3170G>A (p.Ser1057Asn) n.326G>A n.812G>A n.798G>A c.2978G>A (p.Ser993Asn) c.3380G>A (p.Ser1127Asn) | dbSNP |
| 7 | g.87515344T>A | CA368044161 | ABCB1 | c.3169A>T (p.Ser1057Cys) n.325A>T n.811A>T n.797A>T c.2977A>T (p.Ser993Cys) c.3379A>T (p.Ser1127Cys) | |
| 7 | g.87515344T>C | CA368044157 | ABCB1 | c.3169A>G (p.Ser1057Gly) n.325A>G n.811A>G n.797A>G c.2977A>G (p.Ser993Gly) c.3379A>G (p.Ser1127Gly) | |
| 7 | g.87515344T>G | CA368044151 | ABCB1 | c.3169A>C (p.Ser1057Arg) n.325A>C n.811A>C n.797A>C c.2977A>C (p.Ser993Arg) c.3379A>C (p.Ser1127Arg) | |
| 7 | g.87515345C>A | CA456349476 | ABCB1 | c.3168G>T (p.Leu1056=) n.324G>T n.810G>T n.796G>T c.2976G>T (p.Leu992=) c.3378G>T (p.Leu1126=) | |
| 7 | g.87515345C>G | CA456349478 | ABCB1 | c.3168G>C (p.Leu1056=) n.324G>C n.810G>C n.796G>C c.2976G>C (p.Leu992=) c.3378G>C (p.Leu1126=) | |
| 7 | g.87515345C>T | CA456349481 | ABCB1 | c.3168G>A (p.Leu1056=) n.324G>A n.810G>A n.796G>A c.2976G>A (p.Leu992=) c.3378G>A (p.Leu1126=) | |
| 7 | g.87515346A>C | CA368044170 | ABCB1 | c.3167T>G (p.Leu1056Arg) n.323T>G n.809T>G n.795T>G c.2975T>G (p.Leu992Arg) c.3377T>G (p.Leu1126Arg) | gnomAD v4 |
| 7 | g.87515346A>G | CA368044174 | ABCB1 | c.3167T>C (p.Leu1056Pro) n.323T>C n.809T>C n.795T>C c.2975T>C (p.Leu992Pro) c.3377T>C (p.Leu1126Pro) | |
| 7 | g.87515346A>T | CA368044176 | ABCB1 | c.3167T>A (p.Leu1056Gln) n.323T>A n.809T>A n.795T>A c.2975T>A (p.Leu992Gln) c.3377T>A (p.Leu1126Gln) | |
| 7 | g.87515347G>A | CA456349488 | ABCB1 | c.3166C>T (p.Leu1056=) n.322C>T n.808C>T n.794C>T c.2974C>T (p.Leu992=) c.3376C>T (p.Leu1126=) | |
| 7 | g.87515347G>C | CA368044177 | ABCB1 | c.3166C>G (p.Leu1056Val) n.322C>G n.808C>G n.794C>G c.2974C>G (p.Leu992Val) c.3376C>G (p.Leu1126Val) | |
| 7 | g.87515347G>T | CA368044179 | ABCB1 | c.3166C>A (p.Leu1056Met) n.322C>A n.808C>A n.794C>A c.2974C>A (p.Leu992Met) c.3376C>A (p.Leu1126Met) | |
| 7 | g.87515348T>A | CA456349492 | ABCB1 | c.3165A>T (p.Gly1055=) n.321A>T n.807A>T n.793A>T c.2973A>T (p.Gly991=) c.3375A>T (p.Gly1125=) | |
| 7 | g.87515348T>C | CA456349490 | ABCB1 | c.3165A>G (p.Gly1055=) n.321A>G n.807A>G n.793A>G c.2973A>G (p.Gly991=) c.3375A>G (p.Gly1125=) | dbSNP |
| 7 | g.87515348T>G | CA456349491 | ABCB1 | c.3165A>C (p.Gly1055=) n.321A>C n.807A>C n.793A>C c.2973A>C (p.Gly991=) c.3375A>C (p.Gly1125=) | |
| 7 | g.87515348T= | CA1723626185 | ABCB1 | c.3165A= (p.Gly1055=) n.321A= n.807A= n.793A= c.2973A= (p.Gly991=) c.3375A= (p.Gly1125=) | |
| 7 | g.87515349C>A | CA368044186 | ABCB1 | c.3164G>T (p.Gly1055Val) n.320G>T n.806G>T n.792G>T c.2972G>T (p.Gly991Val) c.3374G>T (p.Gly1125Val) | |
| 7 | g.87515349C= | CA1723626186 | ABCB1 | c.3164G= (p.Gly1055=) n.320G= n.806G= n.792G= c.2972G= (p.Gly991=) c.3374G= (p.Gly1125=) | |
| 7 | g.87515349C>G | CA368044192 | ABCB1 | c.3164G>C (p.Gly1055Ala) n.320G>C n.806G>C n.792G>C c.2972G>C (p.Gly991Ala) c.3374G>C (p.Gly1125Ala) | |
| 7 | g.87515349C>T | CA4327838 | ABCB1 | c.3164G>A (p.Gly1055Glu) n.320G>A n.806G>A n.792G>A c.2972G>A (p.Gly991Glu) c.3374G>A (p.Gly1125Glu) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.87515350C>A | CA368044212 | ABCB1 | c.3163G>T (p.Gly1055Ter) n.319G>T n.805G>T n.791G>T c.2971G>T (p.Gly991Ter) c.3373G>T (p.Gly1125Ter) | COSMIC |
| 7 | g.87515350C= | CA1723626187 | ABCB1 | c.3163G= (p.Gly1055=) n.319G= n.805G= n.791G= c.2971G= (p.Gly991=) c.3373G= (p.Gly1125=) | |
| 7 | g.87515350C>G | CA368044217 | ABCB1 | c.3163G>C (p.Gly1055Arg) n.319G>C n.805G>C n.791G>C c.2971G>C (p.Gly991Arg) c.3373G>C (p.Gly1125Arg) | |
| 7 | g.87515350C>T | CA4327839 | ABCB1 | c.3163G>A (p.Gly1055Arg) n.319G>A n.805G>A n.791G>A c.2971G>A (p.Gly991Arg) c.3373G>A (p.Gly1125Arg) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.87515351C>A | CA368044227 | ABCB1 | c.3162G>T (p.Gln1054His) n.318G>T n.804G>T n.790G>T c.2970G>T (p.Gln990His) c.3372G>T (p.Gln1124His) | gnomAD v4 |
| 7 | g.87515351C>G | CA368044229 | ABCB1 | c.3162G>C (p.Gln1054His) n.318G>C n.804G>C n.790G>C c.2970G>C (p.Gln990His) c.3372G>C (p.Gln1124His) | |
| 7 | g.87515351C>T | CA456349513 | ABCB1 | c.3162G>A (p.Gln1054=) n.318G>A n.804G>A n.790G>A c.2970G>A (p.Gln990=) c.3372G>A (p.Gln1124=) | |
| 7 | g.87515352T>A | CA368044233 | ABCB1 | c.3161A>T (p.Gln1054Leu) n.317A>T n.803A>T n.789A>T c.2969A>T (p.Gln990Leu) c.3371A>T (p.Gln1124Leu) | |
| 7 | g.87515352T>C | CA368044241 | ABCB1 | c.3161A>G (p.Gln1054Arg) n.317A>G n.803A>G n.789A>G c.2969A>G (p.Gln990Arg) c.3371A>G (p.Gln1124Arg) | |
| 7 | g.87515352T>G | CA368044232 | ABCB1 | c.3161A>C (p.Gln1054Pro) n.317A>C n.803A>C n.789A>C c.2969A>C (p.Gln990Pro) c.3371A>C (p.Gln1124Pro) | |
| 7 | g.87515353G>A | CA368044247 | ABCB1 | c.3160C>T (p.Gln1054Ter) n.316C>T n.802C>T n.788C>T c.2968C>T (p.Gln990Ter) c.3370C>T (p.Gln1124Ter) | |
| 7 | g.87515353G>C | CA368044252 | ABCB1 | c.3160C>G (p.Gln1054Glu) n.316C>G n.802C>G n.788C>G c.2968C>G (p.Gln990Glu) c.3370C>G (p.Gln1124Glu) | |
| 7 | g.87515353G>T | CA368044268 | ABCB1 | c.3160C>A (p.Gln1054Lys) n.316C>A n.802C>A n.788C>A c.2968C>A (p.Gln990Lys) c.3370C>A (p.Gln1124Lys) | |
| 7 | g.87515354A>C | CA456349533 | ABCB1 | c.3159T>G (p.Leu1053=) n.315T>G n.801T>G n.787T>G c.2967T>G (p.Leu989=) c.3369T>G (p.Leu1123=) | |
| 7 | g.87515354A>G | CA456349532 | ABCB1 | c.3159T>C (p.Leu1053=) n.315T>C n.801T>C n.787T>C c.2967T>C (p.Leu989=) c.3369T>C (p.Leu1123=) | |
| 7 | g.87515354A>T | CA456349534 | ABCB1 | c.3159T>A (p.Leu1053=) n.315T>A n.801T>A n.787T>A c.2967T>A (p.Leu989=) c.3369T>A (p.Leu1123=) | |
| 7 | g.87515355A= | CA1723626188 | ABCB1 | c.3158T= (p.Leu1053=) n.314T= n.800T= n.786T= c.2966T= (p.Leu989=) c.3368T= (p.Leu1123=) | |
| 7 | g.87515355A>C | CA368044271 | ABCB1 | c.3158T>G (p.Leu1053Arg) n.314T>G n.800T>G n.786T>G c.2966T>G (p.Leu989Arg) c.3368T>G (p.Leu1123Arg) | gnomAD v4 |
| 7 | g.87515355A>G | CA368044277 | ABCB1 | c.3158T>C (p.Leu1053Pro) n.314T>C n.800T>C n.786T>C c.2966T>C (p.Leu989Pro) c.3368T>C (p.Leu1123Pro) | dbSNP gnomAD v4 |
| 7 | g.87515355A>T | CA368044286 | ABCB1 | c.3158T>A (p.Leu1053His) n.314T>A n.800T>A n.786T>A c.2966T>A (p.Leu989His) c.3368T>A (p.Leu1123His) | |
| 7 | g.87515356G>A | CA368044290 | ABCB1 | c.3157C>T (p.Leu1053Phe) n.313C>T n.799C>T n.785C>T c.2965C>T (p.Leu989Phe) c.3367C>T (p.Leu1123Phe) | |
| 7 | g.87515356G>C | CA368044305 | ABCB1 | c.3157C>G (p.Leu1053Val) n.313C>G n.799C>G n.785C>G c.2965C>G (p.Leu989Val) c.3367C>G (p.Leu1123Val) | |
| 7 | g.87515356G>T | CA368044314 | ABCB1 | c.3157C>A (p.Leu1053Ile) n.313C>A n.799C>A n.785C>A c.2965C>A (p.Leu989Ile) c.3367C>A (p.Leu1123Ile) | |
| 7 | g.87515357C>A | CA456349545 | ABCB1 | c.3156G>T (p.Val1052=) n.312G>T n.798G>T n.784G>T c.2964G>T (p.Val988=) c.3366G>T (p.Val1122=) | |
| 7 | g.87515357C>G | CA456349546 | ABCB1 | c.3156G>C (p.Val1052=) n.312G>C n.798G>C n.784G>C c.2964G>C (p.Val988=) c.3366G>C (p.Val1122=) | |
| 7 | g.87515357C>T | CA456349547 | ABCB1 | c.3156G>A (p.Val1052=) n.312G>A n.798G>A n.784G>A c.2964G>A (p.Val988=) c.3366G>A (p.Val1122=) | |
| 7 | g.87515358A= | CA1723626189 | ABCB1 | c.3155T= (p.Val1052=) n.311T= n.797T= n.783T= c.2963T= (p.Val988=) c.3365T= (p.Val1122=) | |
| 7 | g.87515358A>C | CA368044329 | ABCB1 | c.3155T>G (p.Val1052Gly) n.311T>G n.797T>G n.783T>G c.2963T>G (p.Val988Gly) c.3365T>G (p.Val1122Gly) | |
| 7 | g.87515358A>G | CA368044330 | ABCB1 | c.3155T>C (p.Val1052Ala) n.311T>C n.797T>C n.783T>C c.2963T>C (p.Val988Ala) c.3365T>C (p.Val1122Ala) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.87515358A>T | CA368044331 | ABCB1 | c.3155T>A (p.Val1052Glu) n.311T>A n.797T>A n.783T>A c.2963T>A (p.Val988Glu) c.3365T>A (p.Val1122Glu) | |
| 7 | g.87515359C>A | CA368044338 | ABCB1 | c.3154G>T (p.Val1052Leu) n.310G>T n.796G>T n.782G>T c.2962G>T (p.Val988Leu) c.3364G>T (p.Val1122Leu) | |
| 7 | g.87515359C>G | CA368044332 | ABCB1 | c.3154G>C (p.Val1052Leu) n.310G>C n.796G>C n.782G>C c.2962G>C (p.Val988Leu) c.3364G>C (p.Val1122Leu) | |
| 7 | g.87515359C>T | CA368044337 | ABCB1 | c.3154G>A (p.Val1052Met) n.310G>A n.796G>A n.782G>A c.2962G>A (p.Val988Met) c.3364G>A (p.Val1122Met) | |
| 7 | g.87515360T>A | CA456349553 | ABCB1 | c.3153A>T (p.Pro1051=) n.309A>T n.795A>T n.781A>T c.2961A>T (p.Pro987=) c.3363A>T (p.Pro1121=) | |
| 7 | g.87515360T>C | CA4327840 | ABCB1 | c.3153A>G (p.Pro1051=) n.309A>G n.795A>G n.781A>G c.2961A>G (p.Pro987=) c.3363A>G (p.Pro1121=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.87515360T>G | CA456349554 | ABCB1 | c.3153A>C (p.Pro1051=) n.309A>C n.795A>C n.781A>C c.2961A>C (p.Pro987=) c.3363A>C (p.Pro1121=) | |
| 7 | g.87515360T= | CA1723626190 | ABCB1 | c.3153A= (p.Pro1051=) n.309A= n.795A= n.781A= c.2961A= (p.Pro987=) c.3363A= (p.Pro1121=) | |
| 7 | g.87515361G>A | CA368044341 | ABCB1 | c.3152C>T (p.Pro1051Leu) n.308C>T n.794C>T n.780C>T c.2960C>T (p.Pro987Leu) c.3362C>T (p.Pro1121Leu) | |
| 7 | g.87515361G>C | CA368044346 | ABCB1 | c.3152C>G (p.Pro1051Arg) n.308C>G n.794C>G n.780C>G c.2960C>G (p.Pro987Arg) c.3362C>G (p.Pro1121Arg) | |
| 7 | g.87515361G>T | CA368044347 | ABCB1 | c.3152C>A (p.Pro1051Gln) n.308C>A n.794C>A n.780C>A c.2960C>A (p.Pro987Gln) c.3362C>A (p.Pro1121Gln) | |
| 7 | g.87515362G>A | CA368044354 | ABCB1 | c.3151C>T (p.Pro1051Ser) n.307C>T n.793C>T n.779C>T c.2959C>T (p.Pro987Ser) c.3361C>T (p.Pro1121Ser) | dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.87515362G>C | CA4327841 | ABCB1 | c.3151C>G (p.Pro1051Ala) n.307C>G n.793C>G n.779C>G c.2959C>G (p.Pro987Ala) c.3361C>G (p.Pro1121Ala) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.87515362G= | CA1723626191 | ABCB1 | c.3151C= (p.Pro1051=) n.307C= n.793C= n.779C= c.2959C= (p.Pro987=) c.3361C= (p.Pro1121=) | |
| 7 | g.87515362G>T | CA368044372 | ABCB1 | c.3151C>A (p.Pro1051Thr) n.307C>A n.793C>A n.779C>A c.2959C>A (p.Pro987Thr) c.3361C>A (p.Pro1121Thr) | |
| 7 | g.87515363G>A | CA456349560 | ABCB1 | c.3150C>T (p.Ile1050=) n.306C>T n.792C>T n.778C>T c.2958C>T (p.Ile986=) c.3360C>T (p.Ile1120=) | gnomAD v4 |
| 7 | g.87515363G>C | CA368044382 | ABCB1 | c.3150C>G (p.Ile1050Met) n.306C>G n.792C>G n.778C>G c.2958C>G (p.Ile986Met) c.3360C>G (p.Ile1120Met) | |
| 7 | g.87515363G>T | CA456349561 | ABCB1 | c.3150C>A (p.Ile1050=) n.306C>A n.792C>A n.778C>A c.2958C>A (p.Ile986=) c.3360C>A (p.Ile1120=) | |
| 7 | g.87515364A>C | CA368044388 | ABCB1 | c.3149T>G (p.Ile1050Ser) n.305T>G n.791T>G n.777T>G c.2957T>G (p.Ile986Ser) c.3359T>G (p.Ile1120Ser) | |
| 7 | g.87515364A>G | CA368044390 | ABCB1 | c.3149T>C (p.Ile1050Thr) n.305T>C n.791T>C n.777T>C c.2957T>C (p.Ile986Thr) c.3359T>C (p.Ile1120Thr) | gnomAD v4 |
| 7 | g.87515364A>T | CA368044393 | ABCB1 | c.3149T>A (p.Ile1050Asn) n.305T>A n.791T>A n.777T>A c.2957T>A (p.Ile986Asn) c.3359T>A (p.Ile1120Asn) | |
| 7 | g.87515365T>A | CA4327842 | ABCB1 | c.3148A>T (p.Ile1050Phe) n.304A>T n.790A>T n.776A>T c.2956A>T (p.Ile986Phe) c.3358A>T (p.Ile1120Phe) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.87515365T>C | CA368044407 | ABCB1 | c.3148A>G (p.Ile1050Val) n.304A>G n.790A>G n.776A>G c.2956A>G (p.Ile986Val) c.3358A>G (p.Ile1120Val) | |
| 7 | g.87515365T>G | CA4327843 | ABCB1 | c.3148A>C (p.Ile1050Leu) n.304A>C n.790A>C n.776A>C c.2956A>C (p.Ile986Leu) c.3358A>C (p.Ile1120Leu) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.87515365T= | CA1723626192 | ABCB1 | c.3148A= (p.Ile1050=) n.304A= n.790A= n.776A= c.2956A= (p.Ile986=) c.3358A= (p.Ile1120=) | |
| 7 | g.87515366G>A | CA4327844 | ABCB1 | c.3147C>T (p.Asp1049=) n.303C>T n.789C>T n.775C>T c.2955C>T (p.Asp985=) c.3357C>T (p.Asp1119=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 7 | g.87515366G>C | CA368044420 | ABCB1 | c.3147C>G (p.Asp1049Glu) n.303C>G n.789C>G n.775C>G c.2955C>G (p.Asp985Glu) c.3357C>G (p.Asp1119Glu) | |
| 7 | g.87515366G= | CA1723626193 | ABCB1 | c.3147C= (p.Asp1049=) n.303C= n.789C= n.775C= c.2955C= (p.Asp985=) c.3357C= (p.Asp1119=) | |
| 7 | g.87515366G>T | CA368044419 | ABCB1 | c.3147C>A (p.Asp1049Glu) n.303C>A n.789C>A n.775C>A c.2955C>A (p.Asp985Glu) c.3357C>A (p.Asp1119Glu) | |
| 7 | g.87515367T>A | CA368044425 | ABCB1 | c.3146A>T (p.Asp1049Val) n.302A>T n.788A>T n.774A>T c.2954A>T (p.Asp985Val) c.3356A>T (p.Asp1119Val) | |
| 7 | g.87515367T>C | CA368044429 | ABCB1 | c.3146A>G (p.Asp1049Gly) n.302A>G n.788A>G n.774A>G c.2954A>G (p.Asp985Gly) c.3356A>G (p.Asp1119Gly) | |
| 7 | g.87515367T>G | CA368044428 | ABCB1 | c.3146A>C (p.Asp1049Ala) n.302A>C n.788A>C n.774A>C c.2954A>C (p.Asp985Ala) c.3356A>C (p.Asp1119Ala) | |
| 7 | g.87515368C>A | CA368044431 | ABCB1 | c.3145G>T (p.Asp1049Tyr) n.301G>T n.787G>T n.773G>T c.2953G>T (p.Asp985Tyr) c.3355G>T (p.Asp1119Tyr) | |
| 7 | g.87515368C>G | CA368044433 | ABCB1 | c.3145G>C (p.Asp1049His) n.301G>C n.787G>C n.773G>C c.2953G>C (p.Asp985His) c.3355G>C (p.Asp1119His) | |
| 7 | g.87515368C>T | CA368044435 | ABCB1 | c.3145G>A (p.Asp1049Asn) n.301G>A n.787G>A n.773G>A c.2953G>A (p.Asp985Asn) c.3355G>A (p.Asp1119Asn) | gnomAD v4 |
| 7 | g.87515369C>A | CA162101590 | ABCB1 | c.3144G>T (p.Pro1048=) n.300G>T n.786G>T n.772G>T c.2952G>T (p.Pro984=) c.3354G>T (p.Pro1118=) | dbSNP |
| 7 | g.87515369C= | CA1723626194 | ABCB1 | c.3144G= (p.Pro1048=) n.300G= n.786G= n.772G= c.2952G= (p.Pro984=) c.3354G= (p.Pro1118=) | |
| 7 | g.87515369C>G | CA456349569 | ABCB1 | c.3144G>C (p.Pro1048=) n.300G>C n.786G>C n.772G>C c.2952G>C (p.Pro984=) c.3354G>C (p.Pro1118=) | |
| 7 | g.87515369C>T | CA456349568 | ABCB1 | c.3144G>A (p.Pro1048=) n.300G>A n.786G>A n.772G>A c.2952G>A (p.Pro984=) c.3354G>A (p.Pro1118=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 7 | g.87515370G>A | CA4327845 | ABCB1 | c.3143C>T (p.Pro1048Leu) n.299C>T n.785C>T n.771C>T c.2951C>T (p.Pro984Leu) c.3353C>T (p.Pro1118Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 7 | g.87515370G>C | CA368044463 | ABCB1 | c.3143C>G (p.Pro1048Arg) n.299C>G n.785C>G n.771C>G c.2951C>G (p.Pro984Arg) c.3353C>G (p.Pro1118Arg) | |
| 7 | g.87515370G= | CA1723626195 | ABCB1 | c.3143C= (p.Pro1048=) n.299C= n.785C= n.771C= c.2951C= (p.Pro984=) c.3353C= (p.Pro1118=) | |
| 7 | g.87515370G>T | CA368044468 | ABCB1 | c.3143C>A (p.Pro1048Gln) n.299C>A n.785C>A n.771C>A c.2951C>A (p.Pro984Gln) c.3353C>A (p.Pro1118Gln) | |
| 7 | g.87515371G>A | CA4327846 | ABCB1 | c.3142C>T (p.Pro1048Ser) n.298C>T n.784C>T n.770C>T c.2950C>T (p.Pro984Ser) c.3352C>T (p.Pro1118Ser) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.87515371G>C | CA368044475 | ABCB1 | c.3142C>G (p.Pro1048Ala) n.298C>G n.784C>G n.770C>G c.2950C>G (p.Pro984Ala) c.3352C>G (p.Pro1118Ala) | |
| 7 | g.87515371G= | CA1723626196 | ABCB1 | c.3142C= (p.Pro1048=) n.298C= n.784C= n.770C= c.2950C= (p.Pro984=) c.3352C= (p.Pro1118=) | |
| 7 | g.87515371G>T | CA368044476 | ABCB1 | c.3142C>A (p.Pro1048Thr) n.298C>A n.784C>A n.770C>A c.2950C>A (p.Pro984Thr) c.3352C>A (p.Pro1118Thr) | |
| 7 | g.87515372T>A | CA456349576 | ABCB1 | c.3141A>T (p.Arg1047=) n.297A>T n.783A>T n.769A>T c.2949A>T (p.Arg983=) c.3351A>T (p.Arg1117=) | |
| 7 | g.87515372T>C | CA456349578 | ABCB1 | c.3141A>G (p.Arg1047=) n.297A>G n.783A>G n.769A>G c.2949A>G (p.Arg983=) c.3351A>G (p.Arg1117=) | |
| 7 | g.87515372T>G | CA456349580 | ABCB1 | c.3141A>C (p.Arg1047=) n.297A>C n.783A>C n.769A>C c.2949A>C (p.Arg983=) c.3351A>C (p.Arg1117=) | dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.87515372T= | CA1723626197 | ABCB1 | c.3141A= (p.Arg1047=) n.297A= n.783A= n.769A= c.2949A= (p.Arg983=) c.3351A= (p.Arg1117=) | |
| 7 | g.87515373C>A | CA368044478 | ABCB1 | c.3140G>T (p.Arg1047Leu) n.296G>T n.782G>T n.768G>T c.2948G>T (p.Arg983Leu) c.3350G>T (p.Arg1117Leu) | gnomAD v4 |
| 7 | g.87515373C= | CA1723626198 | ABCB1 | c.3140G= (p.Arg1047=) n.296G= n.782G= n.768G= c.2948G= (p.Arg983=) c.3350G= (p.Arg1117=) | |
| 7 | g.87515373C>G | CA368044481 | ABCB1 | c.3140G>C (p.Arg1047Pro) n.296G>C n.782G>C n.768G>C c.2948G>C (p.Arg983Pro) c.3350G>C (p.Arg1117Pro) | |
| 7 | g.87515373C>T | CA368044483 | ABCB1 | c.3140G>A (p.Arg1047Gln) n.296G>A n.782G>A n.768G>A c.2948G>A (p.Arg983Gln) c.3350G>A (p.Arg1117Gln) | dbSNP gnomAD v4 |
| 7 | g.87515374G>A | CA4327847 | ABCB1 | c.3139C>T (p.Arg1047Ter) n.295C>T n.781C>T n.767C>T c.2947C>T (p.Arg983Ter) c.3349C>T (p.Arg1117Ter) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.87515374G>C | CA368044484 | ABCB1 | c.3139C>G (p.Arg1047Gly) n.295C>G n.781C>G n.767C>G c.2947C>G (p.Arg983Gly) c.3349C>G (p.Arg1117Gly) | gnomAD v4 |
| 7 | g.87515374G= | CA1723626199 | ABCB1 | c.3139C= (p.Arg1047=) n.295C= n.781C= n.767C= c.2947C= (p.Arg983=) c.3349C= (p.Arg1117=) | |
| 7 | g.87515374G>T | CA456349581 | ABCB1 | c.3139C>A (p.Arg1047=) n.295C>A n.781C>A n.767C>A c.2947C>A (p.Arg983=) c.3349C>A (p.Arg1117=) | |
| 7 | g.87515375G>A | CA456349582 | ABCB1 | c.3138C>T (p.Thr1046=) n.294C>T n.780C>T n.766C>T c.2946C>T (p.Thr982=) c.3348C>T (p.Thr1116=) | |
| 7 | g.87515375G>C | CA456349584 | ABCB1 | c.3138C>G (p.Thr1046=) n.294C>G n.780C>G n.766C>G c.2946C>G (p.Thr982=) c.3348C>G (p.Thr1116=) | gnomAD v4 |
| 7 | g.87515375G= | CA1723626200 | ABCB1 | c.3138C= (p.Thr1046=) n.294C= n.780C= n.766C= c.2946C= (p.Thr982=) c.3348C= (p.Thr1116=) | |
| 7 | g.87515375G>T | CA456349585 | ABCB1 | c.3138C>A (p.Thr1046=) n.294C>A n.780C>A n.766C>A c.2946C>A (p.Thr982=) c.3348C>A (p.Thr1116=) | ClinVar dbSNP |
| 7 | g.87515376G>A | CA368044487 | ABCB1 | c.3137C>T (p.Thr1046Ile) n.293C>T n.779C>T n.765C>T c.2945C>T (p.Thr982Ile) c.3347C>T (p.Thr1116Ile) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.87515376G>C | CA368044489 | ABCB1 | c.3137C>G (p.Thr1046Ser) n.293C>G n.779C>G n.765C>G c.2945C>G (p.Thr982Ser) c.3347C>G (p.Thr1116Ser) | |
| 7 | g.87515376G= | CA1723626201 | ABCB1 | c.3137C= (p.Thr1046=) n.293C= n.779C= n.765C= c.2945C= (p.Thr982=) c.3347C= (p.Thr1116=) | |
| 7 | g.87515376G>T | CA368044493 | ABCB1 | c.3137C>A (p.Thr1046Asn) n.293C>A n.779C>A n.765C>A c.2945C>A (p.Thr982Asn) c.3347C>A (p.Thr1116Asn) | |
| 7 | g.87515377T>A | CA368044499 | ABCB1 | c.3136A>T (p.Thr1046Ser) n.292A>T n.778A>T n.764A>T c.2944A>T (p.Thr982Ser) c.3346A>T (p.Thr1116Ser) | |
| 7 | g.87515377T>C | CA368044506 | ABCB1 | c.3136A>G (p.Thr1046Ala) n.292A>G n.778A>G n.764A>G c.2944A>G (p.Thr982Ala) c.3346A>G (p.Thr1116Ala) | gnomAD v4 |
| 7 | g.87515377T>G | CA4327848 | ABCB1 | c.3136A>C (p.Thr1046Pro) n.292A>C n.778A>C n.764A>C c.2944A>C (p.Thr982Pro) c.3346A>C (p.Thr1116Pro) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.87515377T= | CA1723626202 | ABCB1 | c.3136A= (p.Thr1046=) n.292A= n.778A= n.764A= c.2944A= (p.Thr982=) c.3346A= (p.Thr1116=) | |
| 7 | g.87515378G>A | CA456349637 | ABCB1 | c.3135C>T (p.Pro1045=) n.291C>T n.777C>T n.763C>T c.2943C>T (p.Pro981=) c.3345C>T (p.Pro1115=) | dbSNP gnomAD v4 |
| 7 | g.87515378G>C | CA456349638 | ABCB1 | c.3135C>G (p.Pro1045=) n.291C>G n.777C>G n.763C>G c.2943C>G (p.Pro981=) c.3345C>G (p.Pro1115=) | |
| 7 | g.87515378G= | CA1723626203 | ABCB1 | c.3135C= (p.Pro1045=) n.291C= n.777C= n.763C= c.2943C= (p.Pro981=) c.3345C= (p.Pro1115=) | |
| 7 | g.87515378G>T | CA456349639 | ABCB1 | c.3135C>A (p.Pro1045=) n.291C>A n.777C>A n.763C>A c.2943C>A (p.Pro981=) c.3345C>A (p.Pro1115=) | |
| 7 | g.87515379G>A | CA368044510 | ABCB1 | c.3134C>T (p.Pro1045Leu) n.290C>T n.776C>T n.762C>T c.2942C>T (p.Pro981Leu) c.3344C>T (p.Pro1115Leu) | gnomAD v4 |
| 7 | g.87515379G>C | CA368044513 | ABCB1 | c.3134C>G (p.Pro1045Arg) n.290C>G n.776C>G n.762C>G c.2942C>G (p.Pro981Arg) c.3344C>G (p.Pro1115Arg) | |
| 7 | g.87515379G>T | CA368044519 | ABCB1 | c.3134C>A (p.Pro1045His) n.290C>A n.776C>A n.762C>A c.2942C>A (p.Pro981His) c.3344C>A (p.Pro1115His) | |
| 7 | g.87515380G>A | CA368044525 | ABCB1 | c.3133C>T (p.Pro1045Ser) n.289C>T n.775C>T n.761C>T c.2941C>T (p.Pro981Ser) c.3343C>T (p.Pro1115Ser) | gnomAD v4 |
| 7 | g.87515380G>C | CA162101599 | ABCB1 | c.3133C>G (p.Pro1045Ala) n.289C>G n.775C>G n.761C>G c.2941C>G (p.Pro981Ala) c.3343C>G (p.Pro1115Ala) | dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.87515380G= | CA1723626204 | ABCB1 | c.3133C= (p.Pro1045=) n.289C= n.775C= n.761C= c.2941C= (p.Pro981=) c.3343C= (p.Pro1115=) | |
| 7 | g.87515380G>T | CA368044536 | ABCB1 | c.3133C>A (p.Pro1045Thr) n.289C>A n.775C>A n.761C>A c.2941C>A (p.Pro981Thr) c.3343C>A (p.Pro1115Thr) | dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.87515381A>C | CA368044540 | ABCB1 | c.3132T>G (p.Tyr1044Ter) n.288T>G n.774T>G n.760T>G c.2940T>G (p.Tyr980Ter) c.3342T>G (p.Tyr1114Ter) | |
| 7 | g.87515381A>G | CA456349641 | ABCB1 | c.3132T>C (p.Tyr1044=) n.288T>C n.774T>C n.760T>C c.2940T>C (p.Tyr980=) c.3342T>C (p.Tyr1114=) | |
| 7 | g.87515381A>T | CA368044554 | ABCB1 | c.3132T>A (p.Tyr1044Ter) n.288T>A n.774T>A n.760T>A c.2940T>A (p.Tyr980Ter) c.3342T>A (p.Tyr1114Ter) | |
| 7 | g.87515382T>A | CA4327849 | ABCB1 | c.3131A>T (p.Tyr1044Phe) n.287A>T n.773A>T n.759A>T c.2939A>T (p.Tyr980Phe) c.3341A>T (p.Tyr1114Phe) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.87515382T>C | CA368044562 | ABCB1 | c.3131A>G (p.Tyr1044Cys) n.287A>G n.773A>G n.759A>G c.2939A>G (p.Tyr980Cys) c.3341A>G (p.Tyr1114Cys) | |
| 7 | g.87515382T>G | CA368044566 | ABCB1 | c.3131A>C (p.Tyr1044Ser) n.287A>C n.773A>C n.759A>C c.2939A>C (p.Tyr980Ser) c.3341A>C (p.Tyr1114Ser) | gnomAD v4 |
| 7 | g.87515382T= | CA1723626205 | ABCB1 | c.3131A= (p.Tyr1044=) n.287A= n.773A= n.759A= c.2939A= (p.Tyr980=) c.3341A= (p.Tyr1114=) | |
| 7 | g.87515383A= | CA1723626206 | ABCB1 | c.3130T= (p.Tyr1044=) n.286T= n.772T= n.758T= c.2938T= (p.Tyr980=) c.3340T= (p.Tyr1114=) | |
| 7 | g.87515383A>C | CA368044577 | ABCB1 | c.3130T>G (p.Tyr1044Asp) n.286T>G n.772T>G n.758T>G c.2938T>G (p.Tyr980Asp) c.3340T>G (p.Tyr1114Asp) | |
| 7 | g.87515383A>G | CA368044578 | ABCB1 | c.3130T>C (p.Tyr1044His) n.286T>C n.772T>C n.758T>C c.2938T>C (p.Tyr980His) c.3340T>C (p.Tyr1114His) | dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.87515383A>T | CA368044579 | ABCB1 | c.3130T>A (p.Tyr1044Asn) n.286T>A n.772T>A n.758T>A c.2938T>A (p.Tyr980Asn) c.3340T>A (p.Tyr1114Asn) | |
| 7 | g.87515384G>A | CA456349645 | ABCB1 | c.3129C>T (p.Asn1043=) n.285C>T n.771C>T n.757C>T c.2937C>T (p.Asn979=) c.3339C>T (p.Asn1113=) | |
| 7 | g.87515384G>C | CA368044580 | ABCB1 | c.3129C>G (p.Asn1043Lys) n.285C>G n.771C>G n.757C>G c.2937C>G (p.Asn979Lys) c.3339C>G (p.Asn1113Lys) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.87515384G= | CA1723626207 | ABCB1 | c.3129C= (p.Asn1043=) n.285C= n.771C= n.757C= c.2937C= (p.Asn979=) c.3339C= (p.Asn1113=) | |
| 7 | g.87515384G>T | CA368044582 | ABCB1 | c.3129C>A (p.Asn1043Lys) n.285C>A n.771C>A n.757C>A c.2937C>A (p.Asn979Lys) c.3339C>A (p.Asn1113Lys) | COSMIC |
| 7 | g.87515385T>A | CA368044590 | ABCB1 | c.3128A>T (p.Asn1043Ile) n.284A>T n.770A>T n.756A>T c.2936A>T (p.Asn979Ile) c.3338A>T (p.Asn1113Ile) | |
| 7 | g.87515385T>C | CA368044591 | ABCB1 | c.3128A>G (p.Asn1043Ser) n.284A>G n.770A>G n.756A>G c.2936A>G (p.Asn979Ser) c.3338A>G (p.Asn1113Ser) | |
| 7 | g.87515385T>G | CA368044593 | ABCB1 | c.3128A>C (p.Asn1043Thr) n.284A>C n.770A>C n.756A>C c.2936A>C (p.Asn979Thr) c.3338A>C (p.Asn1113Thr) | |
| 7 | g.87515386T>A | CA368044599 | ABCB1 | c.3127A>T (p.Asn1043Tyr) n.283A>T n.769A>T n.755A>T c.2935A>T (p.Asn979Tyr) c.3337A>T (p.Asn1113Tyr) | |
| 7 | g.87515386T>C | CA368044601 | ABCB1 | c.3127A>G (p.Asn1043Asp) n.283A>G n.769A>G n.755A>G c.2935A>G (p.Asn979Asp) c.3337A>G (p.Asn1113Asp) | gnomAD v4 |
| 7 | g.87515386T>G | CA368044606 | ABCB1 | c.3127A>C (p.Asn1043His) n.283A>C n.769A>C n.755A>C c.2935A>C (p.Asn979His) c.3337A>C (p.Asn1113His) | |
| 7 | g.87515387G>A | CA456349647 | ABCB1 | c.3126C>T (p.Phe1042=) n.282C>T n.768C>T n.754C>T c.2934C>T (p.Phe978=) c.3336C>T (p.Phe1112=) | |
| 7 | g.87515387G>C | CA368044629 | ABCB1 | c.3126C>G (p.Phe1042Leu) n.282C>G n.768C>G n.754C>G c.2934C>G (p.Phe978Leu) c.3336C>G (p.Phe1112Leu) | |
| 7 | g.87515387G>T | CA368044636 | ABCB1 | c.3126C>A (p.Phe1042Leu) n.282C>A n.768C>A n.754C>A c.2934C>A (p.Phe978Leu) c.3336C>A (p.Phe1112Leu) | |
| 7 | g.87515388A>C | CA368044641 | ABCB1 | c.3125T>G (p.Phe1042Cys) n.281T>G n.767T>G n.753T>G c.2933T>G (p.Phe978Cys) c.3335T>G (p.Phe1112Cys) | |
| 7 | g.87515388A>G | CA368044652 | ABCB1 | c.3125T>C (p.Phe1042Ser) n.281T>C n.767T>C n.753T>C c.2933T>C (p.Phe978Ser) c.3335T>C (p.Phe1112Ser) | |
| 7 | g.87515388A>T | CA368044665 | ABCB1 | c.3125T>A (p.Phe1042Tyr) n.281T>A n.767T>A n.753T>A c.2933T>A (p.Phe978Tyr) c.3335T>A (p.Phe1112Tyr) | |
| 7 | g.87515389A>C | CA368044668 | ABCB1 | c.3124T>G (p.Phe1042Val) n.280T>G n.766T>G n.752T>G c.2932T>G (p.Phe978Val) c.3334T>G (p.Phe1112Val) | |
| 7 | g.87515389A>G | CA368044669 | ABCB1 | c.3124T>C (p.Phe1042Leu) n.280T>C n.766T>C n.752T>C c.2932T>C (p.Phe978Leu) c.3334T>C (p.Phe1112Leu) | |
| 7 | g.87515389A>T | CA368044670 | ABCB1 | c.3124T>A (p.Phe1042Ile) n.280T>A n.766T>A n.752T>A c.2932T>A (p.Phe978Ile) c.3334T>A (p.Phe1112Ile) | |
| 7 | g.87515390T>A | CA456349651 | ABCB1 | c.3123A>T (p.Val1041=) n.279A>T n.765A>T n.751A>T c.2931A>T (p.Val977=) c.3333A>T (p.Val1111=) | |
| 7 | g.87515390T>C | CA456349650 | ABCB1 | c.3123A>G (p.Val1041=) n.279A>G n.765A>G n.751A>G c.2931A>G (p.Val977=) c.3333A>G (p.Val1111=) | gnomAD v4 |
| 7 | g.87515390T>G | CA456349649 | ABCB1 | c.3123A>C (p.Val1041=) n.279A>C n.765A>C n.751A>C c.2931A>C (p.Val977=) c.3333A>C (p.Val1111=) | |
| 7 | g.87515391A>C | CA368044671 | ABCB1 | c.3122T>G (p.Val1041Gly) n.278T>G n.764T>G n.750T>G c.2930T>G (p.Val977Gly) c.3332T>G (p.Val1111Gly) | |
| 7 | g.87515391A>G | CA368044674 | ABCB1 | c.3122T>C (p.Val1041Ala) n.278T>C n.764T>C n.750T>C c.2930T>C (p.Val977Ala) c.3332T>C (p.Val1111Ala) | |
| 7 | g.87515391A>T | CA368044684 | ABCB1 | c.3122T>A (p.Val1041Glu) n.278T>A n.764T>A n.750T>A c.2930T>A (p.Val977Glu) c.3332T>A (p.Val1111Glu) | |
| 7 | g.87515392C>A | CA368044691 | ABCB1 | c.3121G>T (p.Val1041Leu) n.277G>T n.763G>T n.749G>T c.2929G>T (p.Val977Leu) c.3331G>T (p.Val1111Leu) | |
| 7 | g.87515392C= | CA1723626208 | ABCB1 | c.3121G= (p.Val1041=) n.277G= n.763G= n.749G= c.2929G= (p.Val977=) c.3331G= (p.Val1111=) | |
| 7 | g.87515392C>G | CA368044694 | ABCB1 | c.3121G>C (p.Val1041Leu) n.277G>C n.763G>C n.749G>C c.2929G>C (p.Val977Leu) c.3331G>C (p.Val1111Leu) | |
| 7 | g.87515392C>T | CA4327850 | ABCB1 | c.3121G>A (p.Val1041Ile) n.277G>A n.763G>A n.749G>A c.2929G>A (p.Val977Ile) c.3331G>A (p.Val1111Ile) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.87515393A>C | CA456349653 | ABCB1 | c.3120T>G (p.Val1040=) n.276T>G n.762T>G n.748T>G c.2928T>G (p.Val976=) c.3330T>G (p.Val1110=) | |
| 7 | g.87515393A>G | CA456349654 | ABCB1 | c.3120T>C (p.Val1040=) n.276T>C n.762T>C n.748T>C c.2928T>C (p.Val976=) c.3330T>C (p.Val1110=) | gnomAD v4 |
| 7 | g.87515393A>T | CA456349655 | ABCB1 | c.3120T>A (p.Val1040=) n.276T>A n.762T>A n.748T>A c.2928T>A (p.Val976=) c.3330T>A (p.Val1110=) | |
| 7 | g.87515394A= | CA1723626209 | ABCB1 | c.3119T= (p.Val1040=) n.275T= n.761T= n.747T= c.2927T= (p.Val976=) c.3329T= (p.Val1110=) | |
| 7 | g.87515394A>C | CA368044701 | ABCB1 | c.3119T>G (p.Val1040Gly) n.275T>G n.761T>G n.747T>G c.2927T>G (p.Val976Gly) c.3329T>G (p.Val1110Gly) | |
| 7 | g.87515394A>G | CA4327851 | ABCB1 | c.3119T>C (p.Val1040Ala) n.275T>C n.761T>C n.747T>C c.2927T>C (p.Val976Ala) c.3329T>C (p.Val1110Ala) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.87515394A>T | CA368044702 | ABCB1 | c.3119T>A (p.Val1040Asp) n.275T>A n.761T>A n.747T>A c.2927T>A (p.Val976Asp) c.3329T>A (p.Val1110Asp) | |
| 7 | g.87515395C>A | CA368044706 | ABCB1 | c.3118G>T (p.Val1040Phe) n.274G>T n.760G>T n.746G>T c.2926G>T (p.Val976Phe) c.3328G>T (p.Val1110Phe) | |
| 7 | g.87515395C>G | CA368044722 | ABCB1 | c.3118G>C (p.Val1040Leu) n.274G>C n.760G>C n.746G>C c.2926G>C (p.Val976Leu) c.3328G>C (p.Val1110Leu) | |
| 7 | g.87515395C>T | CA368044724 | ABCB1 | c.3118G>A (p.Val1040Ile) n.274G>A n.760G>A n.746G>A c.2926G>A (p.Val976Ile) c.3328G>A (p.Val1110Ile) | |
| 7 | g.87515396T>A | CA368044725 | ABCB1 | c.3117A>T (p.Glu1039Asp) n.273A>T n.759A>T n.745A>T c.2925A>T (p.Glu975Asp) c.3327A>T (p.Glu1109Asp) | |
| 7 | g.87515396T>C | CA456349657 | ABCB1 | c.3117A>G (p.Glu1039=) n.273A>G n.759A>G n.745A>G c.2925A>G (p.Glu975=) c.3327A>G (p.Glu1109=) | dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.87515396T>G | CA368044726 | ABCB1 | c.3117A>C (p.Glu1039Asp) n.273A>C n.759A>C n.745A>C c.2925A>C (p.Glu975Asp) c.3327A>C (p.Glu1109Asp) | COSMIC |
| 7 | g.87515396T= | CA1723626210 | ABCB1 | c.3117A= (p.Glu1039=) n.273A= n.759A= n.745A= c.2925A= (p.Glu975=) c.3327A= (p.Glu1109=) | |
| 7 | g.87515397T>A | CA368044741 | ABCB1 | c.3116A>T (p.Glu1039Val) n.272A>T n.758A>T n.744A>T c.2924A>T (p.Glu975Val) c.3326A>T (p.Glu1109Val) | |
| 7 | g.87515397T>C | CA368044735 | ABCB1 | c.3116A>G (p.Glu1039Gly) n.272A>G n.758A>G n.744A>G c.2924A>G (p.Glu975Gly) c.3326A>G (p.Glu1109Gly) | |
| 7 | g.87515397T>G | CA368044729 | ABCB1 | c.3116A>C (p.Glu1039Ala) n.272A>C n.758A>C n.744A>C c.2924A>C (p.Glu975Ala) c.3326A>C (p.Glu1109Ala) | |
| 7 | g.87515398C>A | CA368044744 | ABCB1 | c.3115G>T (p.Glu1039Ter) n.271G>T n.757G>T n.743G>T c.2923G>T (p.Glu975Ter) c.3325G>T (p.Glu1109Ter) | |
| 7 | g.87515398C>G | CA368044750 | ABCB1 | c.3115G>C (p.Glu1039Gln) n.271G>C n.757G>C n.743G>C c.2923G>C (p.Glu975Gln) c.3325G>C (p.Glu1109Gln) | |
| 7 | g.87515398C>T | CA368044751 | ABCB1 | c.3115G>A (p.Glu1039Lys) n.271G>A n.757G>A n.743G>A c.2923G>A (p.Glu975Lys) c.3325G>A (p.Glu1109Lys) | |
| 7 | g.87515399A>C | CA456349661 | ABCB1 | c.3114T>G (p.Gly1038=) n.270T>G n.756T>G n.742T>G c.2922T>G (p.Gly974=) c.3324T>G (p.Gly1108=) | |
| 7 | g.87515399A>G | CA456349662 | ABCB1 | c.3114T>C (p.Gly1038=) n.270T>C n.756T>C n.742T>C c.2922T>C (p.Gly974=) c.3324T>C (p.Gly1108=) | |
| 7 | g.87515399A>T | CA456349663 | ABCB1 | c.3114T>A (p.Gly1038=) n.270T>A n.756T>A n.742T>A c.2922T>A (p.Gly974=) c.3324T>A (p.Gly1108=) | |
| 7 | g.87515400C>A | CA368044754 | ABCB1 | c.3113G>T (p.Gly1038Val) n.269G>T n.755G>T n.741G>T c.2921G>T (p.Gly974Val) c.3323G>T (p.Gly1108Val) | |
| 7 | g.87515400C= | CA1723626211 | ABCB1 | c.3113G= (p.Gly1038=) n.269G= n.755G= n.741G= c.2921G= (p.Gly974=) c.3323G= (p.Gly1108=) | |
| 7 | g.87515400C>G | CA368044757 | ABCB1 | c.3113G>C (p.Gly1038Ala) n.269G>C n.755G>C n.741G>C c.2921G>C (p.Gly974Ala) c.3323G>C (p.Gly1108Ala) | |
| 7 | g.87515400C>T | CA162101605 | ABCB1 | c.3113G>A (p.Gly1038Asp) n.269G>A n.755G>A n.741G>A c.2921G>A (p.Gly974Asp) c.3323G>A (p.Gly1108Asp) | dbSNP |
| 7 | g.87515401C>A | CA368044765 | ABCB1 | c.3112G>T (p.Gly1038Cys) n.268G>T n.754G>T n.740G>T c.2920G>T (p.Gly974Cys) c.3322G>T (p.Gly1108Cys) | |
| 7 | g.87515401C>G | CA368044759 | ABCB1 | c.3112G>C (p.Gly1038Arg) n.268G>C n.754G>C n.740G>C c.2920G>C (p.Gly974Arg) c.3322G>C (p.Gly1108Arg) | |
| 7 | g.87515401C>T | CA368044763 | ABCB1 | c.3112G>A (p.Gly1038Ser) n.268G>A n.754G>A n.740G>A c.2920G>A (p.Gly974Ser) c.3322G>A (p.Gly1108Ser) | |
| 7 | g.87515402A= | CA1723626212 | ABCB1 | c.3111T= (p.Phe1037=) n.267T= n.753T= n.739T= c.2919T= (p.Phe973=) c.3321T= (p.Phe1107=) | |
| 7 | g.87515402A>C | CA368044768 | ABCB1 | c.3111T>G (p.Phe1037Leu) n.267T>G n.753T>G n.739T>G c.2919T>G (p.Phe973Leu) c.3321T>G (p.Phe1107Leu) | |
| 7 | g.87515402A>G | CA456349664 | ABCB1 | c.3111T>C (p.Phe1037=) n.267T>C n.753T>C n.739T>C c.2919T>C (p.Phe973=) c.3321T>C (p.Phe1107=) | |
| 7 | g.87515402A>T | CA4327852 | ABCB1 | c.3111T>A (p.Phe1037Leu) n.267T>A n.753T>A n.739T>A c.2919T>A (p.Phe973Leu) c.3321T>A (p.Phe1107Leu) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |