Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.52678650G>A | CA217474 | KRT1 | c.698C>T (p.Ser233Leu) | ClinVar dbSNP gnomAD v4 |
12 | g.52678650G>C | CA384971697 | KRT1 | c.698C>G (p.Ser233Ter) | dbSNP |
12 | g.52678650G= | CA2036620642 | KRT1 | c.698C= (p.Ser233=) | dbSNP |