Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.87583942C>G | CA1723658197 | ABCB1 | c.286+1570G>C (n.286+1570G>C) c.496+1570G>C (n.496+1570G>C) | dbSNP |
7 | g.87583942C>T | CA12514560 | ABCB1 | c.286+1570G>A (n.286+1570G>A) c.496+1570G>A (n.496+1570G>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |