Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.102070411G>A | CA4410396 | CUX1 | c.262G>A (p.Val88Ile) c.295G>A (p.Val99Ile) c.184G>A (p.Val62Ile) n.366G>A c.247G>A (p.Val83Ile) n.291G>A n.401G>A n.567G>A n.333G>A c.562G>A (p.Val188Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
7 | g.102070411G>C | CA163819971 | CUX1 | c.262G>C (p.Val88Leu) c.295G>C (p.Val99Leu) c.184G>C (p.Val62Leu) n.366G>C c.247G>C (p.Val83Leu) n.291G>C n.401G>C n.567G>C n.333G>C c.562G>C (p.Val188Leu) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |