Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
13 | g.27924341G>T | CA128950 | PDX1 | c.492G>T (p.Glu164Asp) | ClinVar dbSNP |
13 | g.27924341G>A | CA483175674 | PDX1 | c.492G>A (p.Glu164=) | dbSNP gnomAD v4 |
13 | g.27924341G= | CA2080721232 | PDX1 | c.492G= (p.Glu164=) | dbSNP |