Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.41586482G>T | CA399482596 | KRT14 | c.353C>A (p.Thr118Asn) | dbSNP gnomAD v3 gnomAD v4 |
17 | g.41586482G>A | CA16620405 | KRT14 | c.353C>T (p.Thr118Ile) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
17 | g.41586482G= | CA2260086844 | KRT14 | c.353C= (p.Thr118=) | dbSNP |