Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.176094614C>G | CA10576048 | HOXD13 | c.916C>G (p.Arg306Gly) c.859C>G (p.Arg287Gly) | ClinVar dbSNP |
2 | g.176094614C>T | CA124417 | HOXD13 | c.916C>T (p.Arg306Trp) c.859C>T (p.Arg287Trp) | ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC COSMIC |
2 | g.176094614C= | CA1309432019 | HOXD13 | c.916C= (p.Arg306=) c.859C= (p.Arg287=) | dbSNP |