Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
8 | g.31147066T>G | CA174904608 | WRN | c.3397T>G (p.Ser1133Ala) c.*3011T>G (n.*3011T>G) n.2030T>G c.3316T>G (p.Ser1106Ala) c.1798T>G (p.Ser600Ala) n.3670T>G n.614+1442A>C c.3187T>G (p.Ser1063Ala) n.3698T>G | dbSNP |
8 | g.31147066T>A | CA370925206 | WRN | c.3397T>A (p.Ser1133Thr) c.*3011T>A (n.*3011T>A) n.2030T>A c.3316T>A (p.Ser1106Thr) c.1798T>A (p.Ser600Thr) n.3670T>A n.614+1442A>T c.3187T>A (p.Ser1063Thr) n.3698T>A | dbSNP |