Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.115286692G>A | CA1023067 | NGF,NGF-AS1 | c.104C>T (p.Ala35Val) c.-368C>T (n.-368C>T) c.269C>T (p.Ala90Val) n.207+3452G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.115286692G= | CA1139773132 | NGF,NGF-AS1 | c.104C= (p.Ala35=) c.-368C= (n.-368C=) c.269C= (p.Ala90=) n.207+3452G= | dbSNP |