| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 2 | g.51002517G>A | CA48051509 | NRXN1 | c.772+24985C>T (n.772+24985C>T) c.329+24985C>T c.871+23854C>T (n.871+23854C>T) c.297+24985C>T c.301+23854C>T (n.301+23854C>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 2 | g.51002517G= | CA1249865026 | NRXN1 | c.772+24985C= (n.772+24985C=) c.329+24985C= c.871+23854C= (n.871+23854C=) c.297+24985C= c.301+23854C= (n.301+23854C=) | dbSNP |