Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.44907894A>T | CA406303469 | APOE | c.178A>T (p.Thr60Ser) c.256A>T (p.Thr86Ser) | dbSNP |
19 | g.44907894A>G | CA127515 | APOE | c.178A>G (p.Thr60Ala) c.256A>G (p.Thr86Ala) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.44907894A= | CA2338167373 | APOE | c.178A= (p.Thr60=) c.256A= (p.Thr86=) | dbSNP |