Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.88131171G>A | CA357630432 | ABCG2 | c.421C>T (p.Gln141Ter) | dbSNP |
4 | g.88131171G>C | CA357630433 | ABCG2 | c.421C>G (p.Gln141Glu) | dbSNP gnomAD v3 gnomAD v4 |
4 | g.88131171G>T | CA129179 | ABCG2 | c.421C>A (p.Gln141Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.88131171G= | CA1474616670 | ABCG2 | c.421C= (p.Gln141=) | dbSNP dbSNP |