Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.150999023T>G | CA123702 | NOS3 | c.894T>G (p.Asp298Glu) c.276T>G (p.Asp92Glu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.150999023T>A | CA369854472 | NOS3 | c.894T>A (p.Asp298Glu) c.276T>A (p.Asp92Glu) | dbSNP gnomAD v3 gnomAD v4 |
7 | g.150999023T= | CA1630835012 | NOS3 | c.894T= (p.Asp298=) c.276T= (p.Asp92=) | dbSNP |