Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.31576785C>G | CA136866682 | TNF | c.205C>G (p.Arg69Gly) c.251C>G (p.Pro84Arg) | dbSNP gnomAD v4 |
6 | g.31576785C>T | CA3713958 | TNF | c.205C>T (p.Arg69Ter) c.251C>T (p.Pro84Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.31576785C= | CA1619213876 | TNF | c.205C= (p.Arg69=) c.251C= (p.Pro84=) | dbSNP |