Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.13728665G>T | CA379859374 | FAR1 | c.*264G>T (n.*264G>T) c.1439G>T (p.Arg480Leu) c.311G>T (p.Arg104Leu) c.1448G>T (p.Arg483Leu) c.1271G>T (p.Arg424Leu) | ClinVar dbSNP |
11 | g.13728665G>A | CA16042832 | FAR1 | c.*264G>A (n.*264G>A) c.1439G>A (p.Arg480His) c.311G>A (p.Arg104His) c.1448G>A (p.Arg483His) c.1271G>A (p.Arg424His) | ClinVar dbSNP gnomAD v4 |