Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.25302124G>T | CA1352263350 | RARB | c.178+127549G>T (n.178+127549G>T) | dbSNP |
3 | g.25302124G>C | CA1352263351 | RARB | c.178+127549G>C (n.178+127549G>C) | dbSNP |
3 | g.25302124G>A | CA15267382 | RARB | c.178+127549G>A (n.178+127549G>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |