Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.87550185G>A | CA368062508 | ABCB1 | c.1336C>T (p.Pro446Ser) c.1144C>T (p.Pro382Ser) c.1546C>T (p.Pro516Ser) | gnomAD v4 |
7 | g.87550185G>C | CA368062509 | ABCB1 | c.1336C>G (p.Pro446Ala) c.1144C>G (p.Pro382Ala) c.1546C>G (p.Pro516Ala) | |
7 | g.87550185G>T | CA368062510 | ABCB1 | c.1336C>A (p.Pro446Thr) c.1144C>A (p.Pro382Thr) c.1546C>A (p.Pro516Thr) | COSMIC |
7 | g.87550186G>A | CA456450013 | ABCB1 | c.1335C>T (p.Asp445=) c.1143C>T (p.Asp381=) c.1545C>T (p.Asp515=) | gnomAD v4 |
7 | g.87550186G>C | CA368062512 | ABCB1 | c.1335C>G (p.Asp445Glu) c.1143C>G (p.Asp381Glu) c.1545C>G (p.Asp515Glu) | |
7 | g.87550186G>T | CA368062511 | ABCB1 | c.1335C>A (p.Asp445Glu) c.1143C>A (p.Asp381Glu) c.1545C>A (p.Asp515Glu) | |
7 | g.87550187T>A | CA368062513 | ABCB1 | c.1334A>T (p.Asp445Val) c.1142A>T (p.Asp381Val) c.1544A>T (p.Asp515Val) | |
7 | g.87550187T>C | CA368062514 | ABCB1 | c.1334A>G (p.Asp445Gly) c.1142A>G (p.Asp381Gly) c.1544A>G (p.Asp515Gly) | gnomAD v4 |
7 | g.87550187T>G | CA368062515 | ABCB1 | c.1334A>C (p.Asp445Ala) c.1142A>C (p.Asp381Ala) c.1544A>C (p.Asp515Ala) | |
7 | g.87550188C>A | CA368062516 | ABCB1 | c.1333G>T (p.Asp445Tyr) c.1141G>T (p.Asp381Tyr) c.1543G>T (p.Asp515Tyr) | gnomAD v4 |
7 | g.87550188C>G | CA368062517 | ABCB1 | c.1333G>C (p.Asp445His) c.1141G>C (p.Asp381His) c.1543G>C (p.Asp515His) | |
7 | g.87550188C>T | CA368062518 | ABCB1 | c.1333G>A (p.Asp445Asn) c.1141G>A (p.Asp381Asn) c.1543G>A (p.Asp515Asn) | |
7 | g.87550189A>C | CA368062520 | ABCB1 | c.1332T>G (p.Tyr444Ter) c.1140T>G (p.Tyr380Ter) c.1542T>G (p.Tyr514Ter) | |
7 | g.87550189A>G | CA456450014 | ABCB1 | c.1332T>C (p.Tyr444=) c.1140T>C (p.Tyr380=) c.1542T>C (p.Tyr514=) | |
7 | g.87550189A>T | CA368062519 | ABCB1 | c.1332T>A (p.Tyr444Ter) c.1140T>A (p.Tyr380Ter) c.1542T>A (p.Tyr514Ter) | |
7 | g.87550190T>A | CA368062521 | ABCB1 | c.1331A>T (p.Tyr444Phe) c.1139A>T (p.Tyr380Phe) c.1541A>T (p.Tyr514Phe) | |
7 | g.87550190T>C | CA368062522 | ABCB1 | c.1331A>G (p.Tyr444Cys) c.1139A>G (p.Tyr380Cys) c.1541A>G (p.Tyr514Cys) | gnomAD v4 |
7 | g.87550190T>G | CA368062523 | ABCB1 | c.1331A>C (p.Tyr444Ser) c.1139A>C (p.Tyr380Ser) c.1541A>C (p.Tyr514Ser) | |
7 | g.87550191A>C | CA368062524 | ABCB1 | c.1330T>G (p.Tyr444Asp) c.1138T>G (p.Tyr380Asp) c.1540T>G (p.Tyr514Asp) | gnomAD v4 |
7 | g.87550191A>G | CA368062525 | ABCB1 | c.1330T>C (p.Tyr444His) c.1138T>C (p.Tyr380His) c.1540T>C (p.Tyr514His) | |
7 | g.87550191A>T | CA368062526 | ABCB1 | c.1330T>A (p.Tyr444Asn) c.1138T>A (p.Tyr380Asn) c.1540T>A (p.Tyr514Asn) | |
7 | g.87550192G>A | CA456450015 | ABCB1 | c.1329C>T (p.Leu443=) c.1137C>T (p.Leu379=) c.1539C>T (p.Leu513=) | |
7 | g.87550192G>C | CA456450016 | ABCB1 | c.1329C>G (p.Leu443=) c.1137C>G (p.Leu379=) c.1539C>G (p.Leu513=) | |
7 | g.87550192G>T | CA456450017 | ABCB1 | c.1329C>A (p.Leu443=) c.1137C>A (p.Leu379=) c.1539C>A (p.Leu513=) | |
7 | g.87550193A>C | CA368062529 | ABCB1 | c.1328T>G (p.Leu443Arg) c.1136T>G (p.Leu379Arg) c.1538T>G (p.Leu513Arg) | |
7 | g.87550193A>G | CA368062527 | ABCB1 | c.1328T>C (p.Leu443Pro) c.1136T>C (p.Leu379Pro) c.1538T>C (p.Leu513Pro) | |
7 | g.87550193A>T | CA368062528 | ABCB1 | c.1328T>A (p.Leu443His) c.1136T>A (p.Leu379His) c.1538T>A (p.Leu513His) | |
7 | g.87550194G>A | CA4328344 | ABCB1 | c.1327C>T (p.Leu443Phe) c.1135C>T (p.Leu379Phe) c.1537C>T (p.Leu513Phe) | dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.87550194G>C | CA368062530 | ABCB1 | c.1327C>G (p.Leu443Val) c.1135C>G (p.Leu379Val) c.1537C>G (p.Leu513Val) | |
7 | g.87550194G= | CA1723651473 | ABCB1 | c.1327C= (p.Leu443=) c.1135C= (p.Leu379=) c.1537C= (p.Leu513=) | |
7 | g.87550194G>T | CA368062531 | ABCB1 | c.1327C>A (p.Leu443Ile) c.1135C>A (p.Leu379Ile) c.1537C>A (p.Leu513Ile) | ClinVar dbSNP |
7 | g.87550195C>A | CA368062532 | ABCB1 | c.1326G>T (p.Arg442Ser) c.1134G>T (p.Arg378Ser) c.1536G>T (p.Arg512Ser) | |
7 | g.87550195C= | CA1723651475 | ABCB1 | c.1326G= (p.Arg442=) c.1134G= (p.Arg378=) c.1536G= (p.Arg512=) | |
7 | g.87550195C>G | CA368062533 | ABCB1 | c.1326G>C (p.Arg442Ser) c.1134G>C (p.Arg378Ser) c.1536G>C (p.Arg512Ser) | |
7 | g.87550195C>T | CA162123055 | ABCB1 | c.1326G>A (p.Arg442=) c.1134G>A (p.Arg378=) c.1536G>A (p.Arg512=) | dbSNP gnomAD v2 gnomAD v4 |
7 | g.87550196C>A | CA368062536 | ABCB1 | c.1325G>T (p.Arg442Met) c.1133G>T (p.Arg378Met) c.1535G>T (p.Arg512Met) | |
7 | g.87550196C= | CA1723651481 | ABCB1 | c.1325G= (p.Arg442=) c.1133G= (p.Arg378=) c.1535G= (p.Arg512=) | |
7 | g.87550196C>G | CA368062538 | ABCB1 | c.1325G>C (p.Arg442Thr) c.1133G>C (p.Arg378Thr) c.1535G>C (p.Arg512Thr) | ClinVar dbSNP |
7 | g.87550196C>T | CA368062540 | ABCB1 | c.1325G>A (p.Arg442Lys) c.1133G>A (p.Arg378Lys) c.1535G>A (p.Arg512Lys) | |
7 | g.87550197T>A | CA368062543 | ABCB1 | c.1324A>T (p.Arg442Trp) c.1132A>T (p.Arg378Trp) c.1534A>T (p.Arg512Trp) | |
7 | g.87550197T>C | CA368062545 | ABCB1 | c.1324A>G (p.Arg442Gly) c.1132A>G (p.Arg378Gly) c.1534A>G (p.Arg512Gly) | |
7 | g.87550197T>G | CA456359301 | ABCB1 | c.1324A>C (p.Arg442=) c.1132A>C (p.Arg378=) c.1534A>C (p.Arg512=) | |
7 | g.87550198C>A | CA368062549 | ABCB1 | c.1323G>T (p.Gln441His) c.1131G>T (p.Gln377His) c.1533G>T (p.Gln511His) | |
7 | g.87550198C>G | CA368062551 | ABCB1 | c.1323G>C (p.Gln441His) c.1131G>C (p.Gln377His) c.1533G>C (p.Gln511His) | |
7 | g.87550198C>T | CA456359302 | ABCB1 | c.1323G>A (p.Gln441=) c.1131G>A (p.Gln377=) c.1533G>A (p.Gln511=) | |
7 | g.87550199T>A | CA368062555 | ABCB1 | c.1322A>T (p.Gln441Leu) c.1130A>T (p.Gln377Leu) c.1532A>T (p.Gln511Leu) | |
7 | g.87550199T>C | CA368062559 | ABCB1 | c.1322A>G (p.Gln441Arg) c.1130A>G (p.Gln377Arg) c.1532A>G (p.Gln511Arg) | COSMIC |
7 | g.87550199T>G | CA368062557 | ABCB1 | c.1322A>C (p.Gln441Pro) c.1130A>C (p.Gln377Pro) c.1532A>C (p.Gln511Pro) | |
7 | g.87550200G>A | CA368062562 | ABCB1 | c.1321C>T (p.Gln441Ter) c.1129C>T (p.Gln377Ter) c.1531C>T (p.Gln511Ter) | |
7 | g.87550200G>C | CA368062566 | ABCB1 | c.1321C>G (p.Gln441Glu) c.1129C>G (p.Gln377Glu) c.1531C>G (p.Gln511Glu) |