Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.21041028G>C | CA345964124 | APOB | c.293C>G (p.Thr98Ser) c.161C>G (p.Thr54Ser) | dbSNP |
2 | g.21041028G>A | CA022817 | APOB | c.293C>T (p.Thr98Ile) c.161C>T (p.Thr54Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.21041028G= | CA2493490721 | APOB | c.293C= (p.Thr98=) c.161C= (p.Thr54=) | dbSNP |