| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.103049340G>T | CA388605776 | SLC10A2 | c.868C>A (p.Pro290Thr) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.103049340G>A | CA7042015 | SLC10A2 | c.868C>T (p.Pro290Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.103049340G= | CA2115297102 | SLC10A2 | c.868C= (p.Pro290=) | dbSNP |