Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.116822748C>G | CA476868418 | APOA4 | c.87G>C (p.Thr29=) | dbSNP gnomAD v2 gnomAD v4 |
11 | g.116822748C>T | CA6289538 | APOA4 | c.87G>A (p.Thr29=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.116822748C= | CA2002755651 | APOA4 | c.87G= (p.Thr29=) | dbSNP |
11 | g.116822748C>A | CA476868417 | APOA4 | c.87G>T (p.Thr29=) | dbSNP |