Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.49456163C>A | CA364402297 | MMUT | c.828G>T (p.Glu276Asp) | dbSNP gnomAD v2 gnomAD v4 |
6 | g.49456163C>G | CA10575876 | MMUT | c.828G>C (p.Glu276Asp) | ClinVar dbSNP |
6 | g.49456163C>T | CA3847028 | MMUT | c.828G>A (p.Glu276=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.49456163C= | CA1627391404 | MMUT | c.828G= (p.Glu276=) | dbSNP |