Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.116791691G>A | CA6289167 | APOA5 | c.56C>T (p.Ser19Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
11 | g.116791691G>C | CA116845 | APOA5 | c.56C>G (p.Ser19Trp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.116791691G= | CA2002741949 | APOA5 | c.56C= (p.Ser19=) | dbSNP |