| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.103049423G>A | CA031677 | SLC10A2 | c.785C>T (p.Thr262Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.103049423G>T | CA255201947 | SLC10A2 | c.785C>A (p.Thr262Lys) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.103049423G= | CA2115297145 | SLC10A2 | c.785C= (p.Thr262=) | dbSNP |