Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.41586461C>A | CA216925 | KRT14 | c.374G>T (p.Arg125Leu) | ClinVar dbSNP |
17 | g.41586461C>T | CA216921 | KRT14 | c.374G>A (p.Arg125His) | ClinVar dbSNP gnomAD v4 |
17 | g.41586461C>G | CA216923 | KRT14 | c.374G>C (p.Arg125Pro) | ClinVar dbSNP |
17 | g.41586461C= | CA2260086830 | KRT14 | c.374G= (p.Arg125=) | dbSNP |