Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
5 | g.149980653G>T | CA16040994 | SLC26A2 | c.1060G>T (p.Glu354Ter) c.372+2302G>T (n.372+2302G>T) | ClinVar dbSNP |
5 | g.149980653G= | CA1590738470 | SLC26A2 | c.1060G= (p.Glu354=) c.372+2302G= (n.372+2302G=) | dbSNP |