Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.52488338C>T | CA124169 | KRT6A | c.1414G>A (p.Glu472Lys) | ClinVar dbSNP |
12 | g.52488338C= | CA2036520302 | KRT6A | c.1414G= (p.Glu472=) | dbSNP |
12 | g.52488338C>G | CA384953286 | KRT6A | c.1414G>C (p.Glu472Gln) | dbSNP |