Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.87566218C>A | CA123373 | ABCB1 | c.554G>T (p.Gly185Val) c.362G>T (p.Gly121Val) c.764G>T (p.Gly255Val) | ClinVar dbSNP COSMIC |
7 | g.87566218C= | CA1723648216 | ABCB1 | c.554G= (p.Gly185=) c.362G= (p.Gly121=) c.764G= (p.Gly255=) | dbSNP |
7 | g.87566218C>G | CA368090600 | ABCB1 | c.554G>C (p.Gly185Ala) c.362G>C (p.Gly121Ala) c.764G>C (p.Gly255Ala) | dbSNP |