Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.52679785G>C | CA384974914 | KRT1 | c.564C>G (p.Asn188Lys) | ClinVar dbSNP |
12 | g.52679785G>T | CA126049 | KRT1 | c.564C>A (p.Asn188Lys) | ClinVar dbSNP |
12 | g.52679785G= | CA2036598317 | KRT1 | c.564C= (p.Asn188=) | dbSNP |