Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
22 | g.36867434G>T | CA10212936 | NCF4,NCF4-AS1 | c.314G>T (p.Arg105Leu) c.5G>T (p.Arg2Leu) n.619G>T c.488G>T (p.Arg163Leu) c.458G>T (p.Arg153Leu) n.351+2659C>A | dbSNP ExAC gnomAD v2 |
22 | g.36867434G>A | CA129011 | NCF4,NCF4-AS1 | c.314G>A (p.Arg105Gln) c.5G>A (p.Arg2Gln) n.619G>A c.488G>A (p.Arg163Gln) c.458G>A (p.Arg153Gln) n.351+2659C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
22 | g.36867434G>C | CA10212937 | NCF4,NCF4-AS1 | c.314G>C (p.Arg105Pro) c.5G>C (p.Arg2Pro) n.619G>C c.488G>C (p.Arg163Pro) c.458G>C (p.Arg153Pro) n.351+2659C>G | dbSNP ExAC gnomAD v2 gnomAD v4 |