Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.41353007_41353015dup | CA308518766 | TGFB1,TMEM91 | c.30_38dup (p.Leu13_Pro14insLeuLeuLeu) c.-30+1805_-30+1813dup (n.-30+1805_-30+1813dup) n.350+1805_350+1813dup | ClinVar dbSNP |
19 | g.41353010_41353015dup | CA2336426214 | TGFB1,TMEM91 | c.33_38dup (p.Leu13_Pro14insLeuLeu) c.-30+1808_-30+1813dup (n.-30+1808_-30+1813dup) n.350+1808_350+1813dup | dbSNP |
19 | g.41353013_41353015dup | CA2336426217 | TGFB1,TMEM91 | c.36_38dup (p.Leu13_Pro14insLeu) c.-30+1811_-30+1813dup (n.-30+1811_-30+1813dup) n.350+1811_350+1813dup | ClinVar dbSNP |
19 | g.41353015_41353016insAGCAGCAGCAGC | CA2697556602 | TGFB1,TMEM91 | c.38_39insGCTGCTGCTGCT (p.Leu13_Pro14insLeuLeuLeuLeu) c.-30+1813_-30+1814insAGCAGCAGCAGC (n.-30+1813_-30+1814insAGCAGCAGCAGC) n.350+1813_350+1814insAGCAGCAGCAGC | ClinVar dbSNP |