Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.87550493C>A | CA162123283 | ABCB1 | c.1199G>T (p.Ser400Ile) c.1007G>T (p.Ser336Ile) c.1409G>T (p.Ser470Ile) | dbSNP |
7 | g.87550493C= | CA1723651877 | ABCB1 | c.1199G= (p.Ser400=) c.1007G= (p.Ser336=) c.1409G= (p.Ser470=) | |
7 | g.87550493C>G | CA368062997 | ABCB1 | c.1199G>C (p.Ser400Thr) c.1007G>C (p.Ser336Thr) c.1409G>C (p.Ser470Thr) | |
7 | g.87550493C>T | CA200911 | ABCB1 | c.1199G>A (p.Ser400Asn) c.1007G>A (p.Ser336Asn) c.1409G>A (p.Ser470Asn) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.87550494T>A | CA368062998 | ABCB1 | c.1198A>T (p.Ser400Cys) c.1006A>T (p.Ser336Cys) c.1408A>T (p.Ser470Cys) | |
7 | g.87550494T>C | CA368063000 | ABCB1 | c.1198A>G (p.Ser400Gly) c.1006A>G (p.Ser336Gly) c.1408A>G (p.Ser470Gly) | gnomAD v4 |
7 | g.87550494T>G | CA368062999 | ABCB1 | c.1198A>C (p.Ser400Arg) c.1006A>C (p.Ser336Arg) c.1408A>C (p.Ser470Arg) | |
7 | g.87550495G>A | CA456359389 | ABCB1 | c.1197C>T (p.Phe399=) c.1005C>T (p.Phe335=) c.1407C>T (p.Phe469=) | |
7 | g.87550495G>C | CA368063001 | ABCB1 | c.1197C>G (p.Phe399Leu) c.1005C>G (p.Phe335Leu) c.1407C>G (p.Phe469Leu) | |
7 | g.87550495G>T | CA368063003 | ABCB1 | c.1197C>A (p.Phe399Leu) c.1005C>A (p.Phe335Leu) c.1407C>A (p.Phe469Leu) | |
7 | g.87550496A= | CA1723651879 | ABCB1 | c.1196T= (p.Phe399=) c.1004T= (p.Phe335=) c.1406T= (p.Phe469=) | |
7 | g.87550496A>C | CA368063005 | ABCB1 | c.1196T>G (p.Phe399Cys) c.1004T>G (p.Phe335Cys) c.1406T>G (p.Phe469Cys) | |
7 | g.87550496A>G | CA368063008 | ABCB1 | c.1196T>C (p.Phe399Ser) c.1004T>C (p.Phe335Ser) c.1406T>C (p.Phe469Ser) | dbSNP gnomAD v2 |
7 | g.87550496A>T | CA368063007 | ABCB1 | c.1196T>A (p.Phe399Tyr) c.1004T>A (p.Phe335Tyr) c.1406T>A (p.Phe469Tyr) | |
7 | g.87550497A>C | CA368063011 | ABCB1 | c.1195T>G (p.Phe399Val) c.1003T>G (p.Phe335Val) c.1405T>G (p.Phe469Val) | |
7 | g.87550497A>G | CA368063013 | ABCB1 | c.1195T>C (p.Phe399Leu) c.1003T>C (p.Phe335Leu) c.1405T>C (p.Phe469Leu) | |
7 | g.87550497A>T | CA368063014 | ABCB1 | c.1195T>A (p.Phe399Ile) c.1003T>A (p.Phe335Ile) c.1405T>A (p.Phe469Ile) | |
7 | g.87550498G>A | CA456359390 | ABCB1 | c.1194C>T (p.His398=) c.1002C>T (p.His334=) c.1404C>T (p.His468=) | |
7 | g.87550498G>C | CA368063017 | ABCB1 | c.1194C>G (p.His398Gln) c.1002C>G (p.His334Gln) c.1404C>G (p.His468Gln) | |
7 | g.87550498G>T | CA368063018 | ABCB1 | c.1194C>A (p.His398Gln) c.1002C>A (p.His334Gln) c.1404C>A (p.His468Gln) | |
7 | g.87550499T>A | CA4328377 | ABCB1 | c.1193A>T (p.His398Leu) c.1001A>T (p.His334Leu) c.1403A>T (p.His468Leu) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.87550499T>C | CA368063021 | ABCB1 | c.1193A>G (p.His398Arg) c.1001A>G (p.His334Arg) c.1403A>G (p.His468Arg) | |
7 | g.87550499T>G | CA368063023 | ABCB1 | c.1193A>C (p.His398Pro) c.1001A>C (p.His334Pro) c.1403A>C (p.His468Pro) | |
7 | g.87550499T= | CA1723651881 | ABCB1 | c.1193A= (p.His398=) c.1001A= (p.His334=) c.1403A= (p.His468=) | |
7 | g.87550500G>A | CA368063024 | ABCB1 | c.1192C>T (p.His398Tyr) c.1000C>T (p.His334Tyr) c.1402C>T (p.His468Tyr) | |
7 | g.87550500G>C | CA368063026 | ABCB1 | c.1192C>G (p.His398Asp) c.1000C>G (p.His334Asp) c.1402C>G (p.His468Asp) | |
7 | g.87550500G>T | CA368063027 | ABCB1 | c.1192C>A (p.His398Asn) c.1000C>A (p.His334Asn) c.1402C>A (p.His468Asn) | gnomAD v4 |
7 | g.87550501A>C | CA456359391 | ABCB1 | c.1191T>G (p.Val397=) c.999T>G (p.Val333=) c.1401T>G (p.Val467=) | |
7 | g.87550501A>G | CA456359392 | ABCB1 | c.1191T>C (p.Val397=) c.999T>C (p.Val333=) c.1401T>C (p.Val467=) | |
7 | g.87550501A>T | CA456359393 | ABCB1 | c.1191T>A (p.Val397=) c.999T>A (p.Val333=) c.1401T>A (p.Val467=) | |
7 | g.87550502A>C | CA368063029 | ABCB1 | c.1190T>G (p.Val397Gly) c.998T>G (p.Val333Gly) c.1400T>G (p.Val467Gly) | |
7 | g.87550502A>G | CA368063032 | ABCB1 | c.1190T>C (p.Val397Ala) c.998T>C (p.Val333Ala) c.1400T>C (p.Val467Ala) | |
7 | g.87550502A>T | CA368063031 | ABCB1 | c.1190T>A (p.Val397Asp) c.998T>A (p.Val333Asp) c.1400T>A (p.Val467Asp) | |
7 | g.87550503C>A | CA368063035 | ABCB1 | c.1189G>T (p.Val397Phe) c.997G>T (p.Val333Phe) c.1399G>T (p.Val467Phe) | |
7 | g.87550503C= | CA1723651882 | ABCB1 | c.1189G= (p.Val397=) c.997G= (p.Val333=) c.1399G= (p.Val467=) | |
7 | g.87550503C>G | CA368063037 | ABCB1 | c.1189G>C (p.Val397Leu) c.997G>C (p.Val333Leu) c.1399G>C (p.Val467Leu) | gnomAD v4 |
7 | g.87550503C>T | CA4328378 | ABCB1 | c.1189G>A (p.Val397Ile) c.997G>A (p.Val333Ile) c.1399G>A (p.Val467Ile) | dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.87550504A= | CA1723651883 | ABCB1 | c.1188T= (p.Asn396=) c.996T= (p.Asn332=) c.1398T= (p.Asn466=) | |
7 | g.87550504A>C | CA368063041 | ABCB1 | c.1188T>G (p.Asn396Lys) c.996T>G (p.Asn332Lys) c.1398T>G (p.Asn466Lys) | |
7 | g.87550504A>G | CA4328379 | ABCB1 | c.1188T>C (p.Asn396=) c.996T>C (p.Asn332=) c.1398T>C (p.Asn466=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.87550504A>T | CA368063042 | ABCB1 | c.1188T>A (p.Asn396Lys) c.996T>A (p.Asn332Lys) c.1398T>A (p.Asn466Lys) | |
7 | g.87550505T>A | CA368063045 | ABCB1 | c.1187A>T (p.Asn396Ile) c.995A>T (p.Asn332Ile) c.1397A>T (p.Asn466Ile) | |
7 | g.87550505T>C | CA368063046 | ABCB1 | c.1187A>G (p.Asn396Ser) c.995A>G (p.Asn332Ser) c.1397A>G (p.Asn466Ser) | gnomAD v4 |
7 | g.87550505T>G | CA368063048 | ABCB1 | c.1187A>C (p.Asn396Thr) c.995A>C (p.Asn332Thr) c.1397A>C (p.Asn466Thr) | |
7 | g.87550506T>A | CA368063051 | ABCB1 | c.1186A>T (p.Asn396Tyr) c.994A>T (p.Asn332Tyr) c.1396A>T (p.Asn466Tyr) | |
7 | g.87550506T>C | CA368063053 | ABCB1 | c.1186A>G (p.Asn396Asp) c.994A>G (p.Asn332Asp) c.1396A>G (p.Asn466Asp) | |
7 | g.87550506T>G | CA368063050 | ABCB1 | c.1186A>C (p.Asn396His) c.994A>C (p.Asn332His) c.1396A>C (p.Asn466His) | |
7 | g.87550507T>A | CA368063054 | ABCB1 | c.1185A>T (p.Arg395Ser) c.993A>T (p.Arg331Ser) c.1395A>T (p.Arg465Ser) | |
7 | g.87550507T>C | CA456359394 | ABCB1 | c.1185A>G (p.Arg395=) c.993A>G (p.Arg331=) c.1395A>G (p.Arg465=) | |
7 | g.87550507T>G | CA368063055 | ABCB1 | c.1185A>C (p.Arg395Ser) c.993A>C (p.Arg331Ser) c.1395A>C (p.Arg465Ser) |