Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.39504079C>T | CA9432246 | DLL3 | c.661C>T (p.Arg221Ter) c.410-2960C>T (n.410-2960C>T) n.741C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
19 | g.39504079C>G | CA9432245 | DLL3 | c.661C>G (p.Arg221Gly) c.410-2960C>G (n.410-2960C>G) n.741C>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |