| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 1 | g.7829881C>T | CA568575 | PER3 | c.2934C>T (p.Thr978=) c.2907C>T (p.Thr969=) c.2931C>T (p.Thr977=) c.2910C>T (p.Thr970=) c.1974C>T (p.Thr658=) c.2913C>T (p.Thr971=) c.2409C>T (p.Thr803=) c.2766C>T (p.Thr922=) c.2586C>T (p.Thr862=) c.2571C>T (p.Thr857=) c.2928C>T (p.Thr976=) c.2583C>T (p.Thr861=) c.2562C>T (p.Thr854=) c.2565C>T (p.Thr855=) c.2406C>T (p.Thr802=) c.1542C>T (p.Thr514=) c.1539C>T (p.Thr513=) c.2388C>T (p.Thr796=) c.2385C>T (p.Thr795=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.7829881C= | CA1139947026 | PER3 | c.2934C= (p.Thr978=) c.2907C= (p.Thr969=) c.2931C= (p.Thr977=) c.2910C= (p.Thr970=) c.1974C= (p.Thr658=) c.2913C= (p.Thr971=) c.2409C= (p.Thr803=) c.2766C= (p.Thr922=) c.2586C= (p.Thr862=) c.2571C= (p.Thr857=) c.2928C= (p.Thr976=) c.2583C= (p.Thr861=) c.2562C= (p.Thr854=) c.2565C= (p.Thr855=) c.2406C= (p.Thr802=) c.1542C= (p.Thr514=) c.1539C= (p.Thr513=) c.2388C= (p.Thr796=) c.2385C= (p.Thr795=) | dbSNP |