Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.2160956G>C | CA5818205 | INS,INS-IGF2 | c.16C>G (p.Arg6Gly) n.75C>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.2160956G>A | CA123085 | INS,INS-IGF2 | c.16C>T (p.Arg6Cys) n.75C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
11 | g.2160956G= | CA1948027237 | INS,INS-IGF2 | c.16C= (p.Arg6=) n.75C= | dbSNP |