| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.151000245C>A | CA12601064 | NOS3 | c.1132-253C>A (n.1132-253C>A) c.514-253C>A (n.514-253C>A) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.151000245C= | CA1752471509 | NOS3 | c.1132-253C= (n.1132-253C=) c.514-253C= (n.514-253C=) | dbSNP |