Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.11111541C>A | CA10585297 | LDLR | c.1346C>A (p.Thr449Asn) c.1088C>A (p.Thr363Asn) c.968C>A (p.Thr323Asn) c.1342C>A c.584C>A (p.Thr195Asn) c.965C>A (p.Thr322Asn) c.707C>A (p.Thr236Asn) n.87C>A c.568C>A n.1238C>A n.1205C>A | ClinVar dbSNP gnomAD v4 |
19 | g.11111541C>T | CA032045 | LDLR | c.1346C>T (p.Thr449Ile) c.1088C>T (p.Thr363Ile) c.968C>T (p.Thr323Ile) c.1342C>T c.584C>T (p.Thr195Ile) c.965C>T (p.Thr322Ile) c.707C>T (p.Thr236Ile) n.87C>T c.568C>T n.1238C>T n.1205C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |