| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.24285390G>C | CA155829098 | NPY | c.150G>C (p.Ser50=) c.42-29691C>G (n.42-29691C>G) n.473+33967C>G n.345-88361C>G n.345-29691C>G | dbSNP |
| 7 | g.24285390G>T | CA4190743 | NPY | c.150G>T (p.Ser50=) c.42-29691C>A (n.42-29691C>A) n.473+33967C>A n.345-88361C>A n.345-29691C>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.24285390G>A | CA4190742 | NPY | c.150G>A (p.Ser50=) c.42-29691C>T (n.42-29691C>T) n.473+33967C>T n.345-88361C>T n.345-29691C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |