Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.115286135G>T | CA420185241 | NGF,NGF-AS1 | c.661C>A (p.Arg221=) c.190C>A (p.Arg64=) c.826C>A (p.Arg276=) n.207+2895G>T | dbSNP gnomAD v4 |
1 | g.115286135G>A | CA123732 | NGF,NGF-AS1 | c.661C>T (p.Arg221Trp) c.190C>T (p.Arg64Trp) c.826C>T (p.Arg276Trp) n.207+2895G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |