Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g23210 | A10 | 19626605 | C | T | missense_variant | MODERATE | c.3043G>A|p.Glu1015Lys |
S187 |
2 | BAA10g23210 | A10 | 19626849 | G | A | synonymous_variant | LOW | c.2799C>T|p.Tyr933Tyr |
S125 |
3 | BAA10g23210 | A10 | 19626924 | C | T | synonymous_variant | LOW | c.2724G>A|p.Lys908Lys |
S25 |
4 | BAA10g23210 | A10 | 19626944 | C | T | missense_variant | MODERATE | c.2704G>A|p.Ala902Thr |
S18 |
5 | BAA10g23210 | A10 | 19627245 | G | A | synonymous_variant | LOW | c.2403C>T|p.Gly801Gly |
S18 |
6 | BAA10g23210 | A10 | 19627320 | G | A | synonymous_variant | LOW | c.2328C>T|p.Asp776Asp |
S267 |
7 | BAA10g23210 | A10 | 19627802 | C | T | missense_variant | MODERATE | c.1846G>A|p.Ala616Thr |
S249 |
8 | BAA10g23210 | A10 | 19627921 | C | T | missense_variant | MODERATE | c.1727G>A|p.Gly576Glu |
S168 |
9 | BAA10g23210 | A10 | 19628687 | C | T | synonymous_variant | LOW | c.1350G>A|p.Pro450Pro |
S148 S30 S31 |
10 | BAA10g23210 | A10 | 19628692 | C | A | stop_gained | HIGH | c.1345G>T|p.Glu449* |
S278 |
11 | BAA10g23210 | A10 | 19630314 | G | A | synonymous_variant | LOW | c.138C>T|p.Tyr46Tyr |
S298 |
12 | BAA10g23210 | A10 | 19630388 | C | T | missense_variant | MODERATE | c.64G>A|p.Glu22Lys |
S187 |
13 | BAA10g23210 | A10 | 19632188 | C | T | upstream_gene_variant | MODIFIER | c.-1737G>A| |
S44 |
14 | BAA10g23210 | A10 | 19633787 | C | T | upstream_gene_variant | MODIFIER | c.-3336G>A| |
S117 |