| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.93600470C>A | CA377617449 | FFAR4,RBP4 | c.278G>T (p.Gly93Val) c.272G>T (p.Gly91Val) c.697-3604C>A (n.697-3604C>A) | ClinVar dbSNP |
| 10 | g.93600470C>T | CA122833 | FFAR4,RBP4 | c.278G>A (p.Gly93Asp) c.272G>A (p.Gly91Asp) c.697-3604C>T (n.697-3604C>T) | ClinVar dbSNP |
| 10 | g.93600470C= | CA1928692038 | FFAR4,RBP4 | c.278G= (p.Gly93=) c.272G= (p.Gly91=) c.697-3604C= (n.697-3604C=) | dbSNP |