Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.41586462G>C | CA216917 | KRT14 | c.373C>G (p.Arg125Gly) | ClinVar dbSNP |
17 | g.41586462G>T | CA399482518 | KRT14 | c.373C>A (p.Arg125Ser) | ClinVar dbSNP |
17 | g.41586462G>A | CA216919 | KRT14 | c.373C>T (p.Arg125Cys) | ClinVar dbSNP gnomAD v4 |
17 | g.41586462G= | CA2260086831 | KRT14 | c.373C= (p.Arg125=) | dbSNP |