Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g65980 | A03 | 40294491 | C | T | downstream_gene_variant | MODIFIER | c.*4985G>A| |
S264 |
2 | BAA03g65980 | A03 | 40295206 | G | A | downstream_gene_variant | MODIFIER | c.*4270C>T| |
S299 |
3 | BAA03g65980 | A03 | 40297253 | G | A | downstream_gene_variant | MODIFIER | c.*2223C>T| |
S197 |
4 | BAA03g65980 | A03 | 40297518 | G | A | downstream_gene_variant | MODIFIER | c.*1958C>T| |
S295 |
5 | BAA03g65980 | A03 | 40299000 | C | T | downstream_gene_variant | MODIFIER | c.*476G>A| |
S283 |
6 | BAA03g65980 | A03 | 40299142 | G | A | downstream_gene_variant | MODIFIER | c.*334C>T| |
S47 |
7 | BAA03g65980 | A03 | 40299520 | G | A | missense_variant | MODERATE | c.1078C>T|p.Leu360Phe |
S54 |
8 | BAA03g65980 | A03 | 40299788 | C | T | synonymous_variant | LOW | c.810G>A|p.Glu270Glu |
S243 |
9 | BAA03g65980 | A03 | 40299885 | G | A | missense_variant | MODERATE | c.713C>T|p.Thr238Ile |
S296 |
10 | BAA03g65980 | A03 | 40299913 | T | C | missense_variant | MODERATE | c.685A>G|p.Met229Val |
S281 |
11 | BAA03g65980 | A03 | 40299943 | C | T | missense_variant | MODERATE | c.655G>A|p.Ala219Thr |
S243 |
12 | BAA03g65980 | A03 | 40299959 | G | A | synonymous_variant | LOW | c.639C>T|p.Leu213Leu |
S136 |
13 | BAA03g65980 | A03 | 40300008 | G | A | intron_variant | MODIFIER | c.630+28C>T| |
S148 S277 |
14 | BAA03g65980 | A03 | 40304348 | C | T | upstream_gene_variant | MODIFIER | c.-3683G>A| |
S100 |
15 | BAA03g65980 | A03 | 40304672 | G | A | upstream_gene_variant | MODIFIER | c.-4007C>T| |
S218 S234 |
16 | BAA03g65980 | A03 | 40304990 | G | A | upstream_gene_variant | MODIFIER | c.-4325C>T| |
S1 S90 |
17 | BAA03g65980 | A03 | 40305278 | C | T | upstream_gene_variant | MODIFIER | c.-4613G>A| |
S103 |