Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.24285260T>A | CA4190722 | NPY | c.20T>A (p.Leu7Gln) c.42-29561A>T (n.42-29561A>T) n.473+34097A>T n.345-88231A>T n.345-29561A>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.24285260T>C | CA123720 | NPY | c.20T>C (p.Leu7Pro) c.42-29561A>G (n.42-29561A>G) n.473+34097A>G n.345-88231A>G n.345-29561A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |