| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.93600739A>T | CA122832 | FFAR4,RBP4 | c.176T>A (p.Ile59Asn) c.170T>A (p.Ile57Asn) c.697-3335A>T (n.697-3335A>T) | ClinVar dbSNP gnomAD v4 |
| 10 | g.93600739A>G | CA377618316 | FFAR4,RBP4 | c.176T>C (p.Ile59Thr) c.170T>C (p.Ile57Thr) c.697-3335A>G (n.697-3335A>G) | dbSNP gnomAD v4 |
| 10 | g.93600739A= | CA1928692374 | FFAR4,RBP4 | c.176T= (p.Ile59=) c.170T= (p.Ile57=) c.697-3335A= (n.697-3335A=) | dbSNP |