Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.87550285A=CA1630834805ABCB1c.1236T= (p.Gly412=)
c.1044T= (p.Gly348=)
c.1446T= (p.Gly482=)
7g.87550285A>CCA456359367ABCB1c.1236T>G (p.Gly412=)
c.1044T>G (p.Gly348=)
c.1446T>G (p.Gly482=)
7g.87550285A>GCA201020ABCB1c.1236T>C (p.Gly412=)
c.1044T>C (p.Gly348=)
c.1446T>C (p.Gly482=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.87550285A>TCA456359366ABCB1c.1236T>A (p.Gly412=)
c.1044T>A (p.Gly348=)
c.1446T>A (p.Gly482=)
7g.87550286C>ACA368062907ABCB1c.1235G>T (p.Gly412Val)
c.1043G>T (p.Gly348Val)
c.1445G>T (p.Gly482Val)
7g.87550286C>GCA368062908ABCB1c.1235G>C (p.Gly412Ala)
c.1043G>C (p.Gly348Ala)
c.1445G>C (p.Gly482Ala)
7g.87550286C>TCA368062909ABCB1c.1235G>A (p.Gly412Asp)
c.1043G>A (p.Gly348Asp)
c.1445G>A (p.Gly482Asp)
7g.87550287C>ACA368062910ABCB1c.1234G>T (p.Gly412Cys)
c.1042G>T (p.Gly348Cys)
c.1444G>T (p.Gly482Cys)
7g.87550287C=CA1723651637ABCB1c.1234G= (p.Gly412=)
c.1042G= (p.Gly348=)
c.1444G= (p.Gly482=)
7g.87550287C>GCA368062911ABCB1c.1234G>C (p.Gly412Arg)
c.1042G>C (p.Gly348Arg)
c.1444G>C (p.Gly482Arg)
dbSNP
7g.87550287C>TCA368062912ABCB1c.1234G>A (p.Gly412Ser)
c.1042G>A (p.Gly348Ser)
c.1444G>A (p.Gly482Ser)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.87550288C>ACA368062913ABCB1c.1233G>T (p.Lys411Asn)
c.1041G>T (p.Lys347Asn)
c.1443G>T (p.Lys481Asn)
7g.87550288C=CA1723651639ABCB1c.1233G= (p.Lys411=)
c.1041G= (p.Lys347=)
c.1443G= (p.Lys481=)
7g.87550288C>GCA368062914ABCB1c.1233G>C (p.Lys411Asn)
c.1041G>C (p.Lys347Asn)
c.1443G>C (p.Lys481Asn)
gnomAD v4
7g.87550288C>TCA162123136ABCB1c.1233G>A (p.Lys411=)
c.1041G>A (p.Lys347=)
c.1443G>A (p.Lys481=)
dbSNP gnomAD v2 gnomAD v4
7g.87550289T>ACA368062917ABCB1c.1232A>T (p.Lys411Met)
c.1040A>T (p.Lys347Met)
c.1442A>T (p.Lys481Met)
7g.87550289T>CCA368062915ABCB1c.1232A>G (p.Lys411Arg)
c.1040A>G (p.Lys347Arg)
c.1442A>G (p.Lys481Arg)
7g.87550289T>GCA368062916ABCB1c.1232A>C (p.Lys411Thr)
c.1040A>C (p.Lys347Thr)
c.1442A>C (p.Lys481Thr)
7g.87550290T>ACA368062918ABCB1c.1231A>T (p.Lys411Ter)
c.1039A>T (p.Lys347Ter)
c.1441A>T (p.Lys481Ter)
7g.87550290T>CCA368062919ABCB1c.1231A>G (p.Lys411Glu)
c.1039A>G (p.Lys347Glu)
c.1441A>G (p.Lys481Glu)
7g.87550290T>GCA368062920ABCB1c.1231A>C (p.Lys411Gln)
c.1039A>C (p.Lys347Gln)
c.1441A>C (p.Lys481Gln)
7g.87550291C>ACA368062921ABCB1c.1230G>T (p.Leu410Phe)
c.1038G>T (p.Leu346Phe)
c.1440G>T (p.Leu480Phe)
7g.87550291C>GCA368062922ABCB1c.1230G>C (p.Leu410Phe)
c.1038G>C (p.Leu346Phe)
c.1440G>C (p.Leu480Phe)
7g.87550291C>TCA456359368ABCB1c.1230G>A (p.Leu410=)
c.1038G>A (p.Leu346=)
c.1440G>A (p.Leu480=)
7g.87550292A=CA1723651642ABCB1c.1229T= (p.Leu410=)
c.1037T= (p.Leu346=)
c.1439T= (p.Leu480=)
7g.87550292A>CCA368062923ABCB1c.1229T>G (p.Leu410Trp)
c.1037T>G (p.Leu346Trp)
c.1439T>G (p.Leu480Trp)
7g.87550292A>GCA162123137ABCB1c.1229T>C (p.Leu410Ser)
c.1037T>C (p.Leu346Ser)
c.1439T>C (p.Leu480Ser)
dbSNP gnomAD v4
7g.87550292A>TCA368062924ABCB1c.1229T>A (p.Leu410Ter)
c.1037T>A (p.Leu346Ter)
c.1439T>A (p.Leu480Ter)
7g.87550293A>CCA368062925ABCB1c.1228T>G (p.Leu410Val)
c.1036T>G (p.Leu346Val)
c.1438T>G (p.Leu480Val)
7g.87550293A>GCA456359369ABCB1c.1228T>C (p.Leu410=)
c.1036T>C (p.Leu346=)
c.1438T>C (p.Leu480=)
7g.87550293A>TCA368062926ABCB1c.1228T>A (p.Leu410Met)
c.1036T>A (p.Leu346Met)
c.1438T>A (p.Leu480Met)
7g.87550294G>ACA456359370ABCB1c.1227C>T (p.Ile409=)
c.1035C>T (p.Ile345=)
c.1437C>T (p.Ile479=)
COSMIC
7g.87550294G>CCA368062927ABCB1c.1227C>G (p.Ile409Met)
c.1035C>G (p.Ile345Met)
c.1437C>G (p.Ile479Met)
7g.87550294G>TCA456359371ABCB1c.1227C>A (p.Ile409=)
c.1035C>A (p.Ile345=)
c.1437C>A (p.Ile479=)
7g.87550295A=CA1723651644ABCB1c.1226T= (p.Ile409=)
c.1034T= (p.Ile345=)
c.1436T= (p.Ile479=)
7g.87550295A>CCA368062930ABCB1c.1226T>G (p.Ile409Ser)
c.1034T>G (p.Ile345Ser)
c.1436T>G (p.Ile479Ser)
7g.87550295A>GCA368062929ABCB1c.1226T>C (p.Ile409Thr)
c.1034T>C (p.Ile345Thr)
c.1436T>C (p.Ile479Thr)
gnomAD v4
7g.87550295A>TCA368062928ABCB1c.1226T>A (p.Ile409Asn)
c.1034T>A (p.Ile345Asn)
c.1436T>A (p.Ile479Asn)
dbSNP gnomAD v2 gnomAD v4
7g.87550296T>ACA368062931ABCB1c.1225A>T (p.Ile409Phe)
c.1033A>T (p.Ile345Phe)
c.1435A>T (p.Ile479Phe)
ClinVar dbSNP
7g.87550296T>CCA368062932ABCB1c.1225A>G (p.Ile409Val)
c.1033A>G (p.Ile345Val)
c.1435A>G (p.Ile479Val)
7g.87550296T>GCA368062933ABCB1c.1225A>C (p.Ile409Leu)
c.1033A>C (p.Ile345Leu)
c.1435A>C (p.Ile479Leu)
7g.87550296T=CA1723651648ABCB1c.1225A= (p.Ile409=)
c.1033A= (p.Ile345=)
c.1435A= (p.Ile479=)
7g.87550297C>ACA368062934ABCB1c.1225-1G>T (n.1225-1G>T)
c.1033-1G>T (n.1033-1G>T)
c.1435-1G>T (n.1435-1G>T)
7g.87550297C>GCA368062935ABCB1c.1225-1G>C (n.1225-1G>C)
c.1033-1G>C (n.1033-1G>C)
c.1435-1G>C (n.1435-1G>C)
7g.87550297C>TCA368062936ABCB1c.1225-1G>A (n.1225-1G>A)
c.1033-1G>A (n.1033-1G>A)
c.1435-1G>A (n.1435-1G>A)
7g.87550298T>ACA368062937ABCB1c.1225-2A>T (n.1225-2A>T)
c.1033-2A>T (n.1033-2A>T)
c.1435-2A>T (n.1435-2A>T)
7g.87550298T>CCA368062938ABCB1c.1225-2A>G (n.1225-2A>G)
c.1033-2A>G (n.1033-2A>G)
c.1435-2A>G (n.1435-2A>G)
7g.87550298T>GCA368062939ABCB1c.1225-2A>C (n.1225-2A>C)
c.1033-2A>C (n.1033-2A>C)
c.1435-2A>C (n.1435-2A>C)
7g.87550299A=CA1723651650ABCB1c.1225-3T= (n.1225-3T=)
c.1033-3T= (n.1033-3T=)
c.1435-3T= (n.1435-3T=)
7g.87550299A>GCA843388999ABCB1c.1225-3T>C (n.1225-3T>C)
c.1033-3T>C (n.1033-3T>C)
c.1435-3T>C (n.1435-3T>C)
dbSNP gnomAD v3 gnomAD v4

Number of alleles fetched