Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.124397955A>T | CA144139 | OAT | c.1307T>A (p.Ile436Asn) c.893T>A (p.Ile298Asn) c.986T>A (p.Ile329Asn) c.707T>A (p.Ile236Asn) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.124397955A= | CA1942335632 | OAT | c.1307T= (p.Ile436=) c.893T= (p.Ile298=) c.986T= (p.Ile329=) c.707T= (p.Ile236=) | dbSNP |