Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.119320747T>A | CA104693458 | FABP2 | c.163A>T (p.Thr55Ser) | dbSNP gnomAD v4 |
4 | g.119320747T>C | CA126561 | FABP2 | c.163A>G (p.Thr55Ala) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.119320747T>G | CA104693464 | FABP2 | c.163A>C (p.Thr55Pro) | dbSNP gnomAD v4 |
4 | g.119320747T= | CA1488878540 | FABP2 | c.163A= (p.Thr55=) | dbSNP |