Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
16 | g.56871520T>C | CA14221079 | SLC12A3 | c.852+784T>C (n.852+784T>C) c.849+784T>C (n.849+784T>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.56871520T>A | CA2224349995 | SLC12A3 | c.852+784T>A (n.852+784T>A) c.849+784T>A (n.849+784T>A) | dbSNP |