Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.41612306A>T | CA217386 | KRT16 | c.383T>A (p.Leu128Gln) n.460T>A c.-312-20T>A (n.-312-20T>A) | ClinVar dbSNP |
17 | g.41612306A>G | CA10588648 | KRT16 | c.383T>C (p.Leu128Pro) n.460T>C c.-312-20T>C (n.-312-20T>C) | ClinVar dbSNP |
17 | g.41612306A= | CA2260099688 | KRT16 | c.383T= (p.Leu128=) n.460T= c.-312-20T= (n.-312-20T=) | dbSNP |