Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.21176793A>CCA384104774SLCO1B1c.377A>C (p.Glu126Ala)
c.443A>C
gnomAD v4
12g.21176793A>GCA384104775SLCO1B1c.377A>G (p.Glu126Gly)
c.443A>G
gnomAD v4
12g.21176793A>TCA384104776SLCO1B1c.377A>T (p.Glu126Val)
c.443A>T
12g.21176794A>CCA384104777SLCO1B1c.378A>C (p.Glu126Asp)
c.444A>C
gnomAD v4
12g.21176794A>GCA478866753SLCO1B1c.378A>G (p.Glu126=)
c.444A>G
12g.21176794A>TCA384104778SLCO1B1c.378A>T (p.Glu126Asp)
c.444A>T
12g.21176795A>CCA384104779SLCO1B1c.379A>C (p.Thr127Pro)
c.445A>C
gnomAD v4
12g.21176795A>GCA384104780SLCO1B1c.379A>G (p.Thr127Ala)
c.445A>G
12g.21176795A>TCA384104781SLCO1B1c.379A>T (p.Thr127Ser)
c.445A>T
COSMIC
12g.21176796C>ACA384104782SLCO1B1c.380C>A (p.Thr127Asn)
c.446C>A
gnomAD v4
12g.21176796C=CA2020990592SLCO1B1c.380C= (p.Thr127=)
c.446C=
12g.21176796C>GCA6476670SLCO1B1c.380C>G (p.Thr127Ser)
c.446C>G
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.21176796C>TCA384104783SLCO1B1c.380C>T (p.Thr127Ile)
c.446C>T
12g.21176797T>ACA6476671SLCO1B1c.381T>A (p.Thr127=)
c.447T>A
dbSNP ExAC gnomAD v2 gnomAD v4
12g.21176797T>CCA478866756SLCO1B1c.381T>C (p.Thr127=)
c.447T>C
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.21176797T>GCA478866757SLCO1B1c.381T>G (p.Thr127=)
c.447T>G
12g.21176797T=CA2020990593SLCO1B1c.381T= (p.Thr127=)
c.447T=
12g.21176798A>CCA384104785SLCO1B1c.382A>C (p.Asn128His)
c.448A>C
ClinVar gnomAD v4
12g.21176798A>GCA384104784SLCO1B1c.382A>G (p.Asn128Asp)
c.448A>G
gnomAD v4
12g.21176798A>TCA384104786SLCO1B1c.382A>T (p.Asn128Tyr)
c.448A>T
gnomAD v4
12g.21176799A>CCA384104787SLCO1B1c.383A>C (p.Asn128Thr)
c.449A>C
12g.21176799A>GCA384104789SLCO1B1c.383A>G (p.Asn128Ser)
c.449A>G
12g.21176799A>TCA384104788SLCO1B1c.383A>T (p.Asn128Ile)
c.449A>T
12g.21176800T>ACA384104790SLCO1B1c.384T>A (p.Asn128Lys)
c.450T>A
12g.21176800T>CCA6476672SLCO1B1c.384T>C (p.Asn128=)
c.450T>C
dbSNP ExAC gnomAD v2 gnomAD v4
12g.21176800T>GCA384104791SLCO1B1c.384T>G (p.Asn128Lys)
c.450T>G
12g.21176800T=CA2020990594SLCO1B1c.384T= (p.Asn128=)
c.450T=
12g.21176801A=CA2020990595SLCO1B1c.385A= (p.Ile129=)
c.451A=
12g.21176801A>CCA384104792SLCO1B1c.385A>C (p.Ile129Leu)
c.451A>C
12g.21176801A>GCA6476673SLCO1B1c.385A>G (p.Ile129Val)
c.451A>G
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.21176801A>TCA384104793SLCO1B1c.385A>T (p.Ile129Phe)
c.451A>T
12g.21176802T>ACA384104794SLCO1B1c.386T>A (p.Ile129Asn)
c.452T>A
gnomAD v4
12g.21176802T>CCA384104795SLCO1B1c.386T>C (p.Ile129Thr)
c.452T>C
gnomAD v4
12g.21176802T>GCA384104796SLCO1B1c.386T>G (p.Ile129Ser)
c.452T>G
12g.21176803C>ACA478866762SLCO1B1c.387C>A (p.Ile129=)
c.453C>A
gnomAD v4
12g.21176803C>GCA384104797SLCO1B1c.387C>G (p.Ile129Met)
c.453C>G
12g.21176803C>TCA478866763SLCO1B1c.387C>T (p.Ile129=)
c.453C>T
dbSNP gnomAD v4 COSMIC
12g.21176804A=CA1630855540SLCO1B1c.388A= (p.Asn130=)
c.454A=
12g.21176804A>CCA384104798SLCO1B1c.388A>C (p.Asn130His)
c.454A>C
dbSNP gnomAD v4
12g.21176804A>GCA6476674SLCO1B1c.388A>G (p.Asn130Asp)
c.454A>G
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.21176804A>TCA384104799SLCO1B1c.388A>T (p.Asn130Tyr)
c.454A>T
dbSNP gnomAD v3 gnomAD v4
12g.21176804_21176805delCA2617896114SLCO1B1c.388_389del (p.Asn130PhefsTer15)
c.454_455del
gnomAD v4
12g.21176804_21176805insGCA945497069SLCO1B1c.388_389insG (p.Asn130ArgfsTer16)
c.454_455insG
gnomAD v3 gnomAD v4
12g.21176805A>CCA384104800SLCO1B1c.389A>C (p.Asn130Thr)
c.455A>C
12g.21176805A>GCA384104801SLCO1B1c.389A>G (p.Asn130Ser)
c.455A>G
gnomAD v4
12g.21176805A>TCA384104802SLCO1B1c.389A>T (p.Asn130Ile)
c.455A>T
12g.21176806T>ACA384104803SLCO1B1c.390T>A (p.Asn130Lys)
c.456T>A
12g.21176806T>CCA478866765SLCO1B1c.390T>C (p.Asn130=)
c.456T>C
gnomAD v4
12g.21176806T>GCA384104804SLCO1B1c.390T>G (p.Asn130Lys)
c.456T>G
COSMIC
12g.21176807T>ACA384104805SLCO1B1c.391T>A (p.Ser131Thr)
c.457T>A

Number of alleles fetched