| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.44873027C>G | CA14644142 | NECTIN2 | c.775+878C>G (n.775+878C>G) c.297+878C>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.44873027C>T | CA882665495 | NECTIN2 | c.775+878C>T (n.775+878C>T) c.297+878C>T | dbSNP gnomAD v3 gnomAD v4 |
| 19 | g.44873027C>A | CA2338149738 | NECTIN2 | c.775+878C>A (n.775+878C>A) c.297+878C>A | dbSNP |