Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.116821618C>A | CA382702370 | APOA4 | c.440G>T (p.Ser147Ile) | dbSNP |
11 | g.116821618C>G | CA382702373 | APOA4 | c.440G>C (p.Ser147Thr) | dbSNP |
11 | g.116821618C>T | CA6289428 | APOA4 | c.440G>A (p.Ser147Asn) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.116821618C= | CA2002755128 | APOA4 | c.440G= (p.Ser147=) | dbSNP |