Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g17630 | A06 | 8975416 | G | A | downstream_gene_variant | MODIFIER | c.*4105C>T| |
S64 |
2 | BAA06g17630 | A06 | 8975602 | C | T | downstream_gene_variant | MODIFIER | c.*3919G>A| |
S65 |
3 | BAA06g17630 | A06 | 8975906 | G | A | downstream_gene_variant | MODIFIER | c.*3615C>T| |
S95 |
4 | BAA06g17630 | A06 | 8976026 | C | T | downstream_gene_variant | MODIFIER | c.*3495G>A| |
S286 |
5 | BAA06g17630 | A06 | 8976255 | G | A | downstream_gene_variant | MODIFIER | c.*3266C>T| |
S208 S219 |
6 | BAA06g17630 | A06 | 8976856 | G | A | downstream_gene_variant | MODIFIER | c.*2665C>T| |
S158 S308 |
7 | BAA06g17630 | A06 | 8977053 | C | T | downstream_gene_variant | MODIFIER | c.*2468G>A| |
S124 |
8 | BAA06g17630 | A06 | 8977277 | C | T | downstream_gene_variant | MODIFIER | c.*2244G>A| |
S65 |
9 | BAA06g17630 | A06 | 8977656 | G | A | downstream_gene_variant | MODIFIER | c.*1865C>T| |
S165 |
10 | BAA06g17630 | A06 | 8977838 | C | T | downstream_gene_variant | MODIFIER | c.*1683G>A| |
S98 |
11 | BAA06g17630 | A06 | 8978098 | C | T | downstream_gene_variant | MODIFIER | c.*1423G>A| |
S179 |
12 | BAA06g17630 | A06 | 8978193 | G | A | downstream_gene_variant | MODIFIER | c.*1328C>T| |
S95 |
13 | BAA06g17630 | A06 | 8978257 | C | T | downstream_gene_variant | MODIFIER | c.*1264G>A| |
S142 |
14 | BAA06g17630 | A06 | 8978299 | C | T | downstream_gene_variant | MODIFIER | c.*1222G>A| |
S245 |
15 | BAA06g17630 | A06 | 8978323 | G | A | downstream_gene_variant | MODIFIER | c.*1198C>T| |
S210 |
16 | BAA06g17630 | A06 | 8978384 | C | T | downstream_gene_variant | MODIFIER | c.*1137G>A| |
S6 |
17 | BAA06g17630 | A06 | 8979163 | G | A | downstream_gene_variant | MODIFIER | c.*358C>T| |
S206 S26 |
18 | BAA06g17630 | A06 | 8979605 | G | A | synonymous_variant | LOW | c.3120C>T|p.Thr1040Thr |
S117 |
19 | BAA06g17630 | A06 | 8981341 | G | A | missense_variant | MODERATE | c.2437C>T|p.Leu813Phe |
S77 |
20 | BAA06g17630 | A06 | 8981720 | G | A | synonymous_variant | LOW | c.2058C>T|p.Asn686Asn |
S136 |
21 | BAA06g17630 | A06 | 8982615 | G | A | missense_variant | MODERATE | c.1457C>T|p.Thr486Ile |
S8 |
22 | BAA06g17630 | A06 | 8983033 | G | A | missense_variant | MODERATE | c.1039C>T|p.Pro347Ser |
S82 S92 |
23 | BAA06g17630 | A06 | 8984236 | C | T | upstream_gene_variant | MODIFIER | c.-165G>A| |
S223 |
24 | BAA06g17630 | A06 | 8984365 | G | A | upstream_gene_variant | MODIFIER | c.-294C>T| |
S85 |
25 | BAA06g17630 | A06 | 8984982 | G | A | upstream_gene_variant | MODIFIER | c.-911C>T| |
S35 |