| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 21 | g.21115536A>T | CA318666400 | NCAM2 | c.55+116918A>T (n.55+116918A>T) c.-21-95005A>T (n.-21-95005A>T) c.-450+116918A>T (n.-450+116918A>T) | dbSNP |
| 21 | g.21115536A>C | CA318666399 | NCAM2 | c.55+116918A>C (n.55+116918A>C) c.-21-95005A>C (n.-21-95005A>C) c.-450+116918A>C (n.-450+116918A>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |