Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g06230 | A04 | 4068504 | G | A | upstream_gene_variant | MODIFIER | c.-4659G>A| |
S280 |
2 | BAA04g06230 | A04 | 4068519 | C | T | upstream_gene_variant | MODIFIER | c.-4644C>T| |
S167 |
3 | BAA04g06230 | A04 | 4069039 | C | T | upstream_gene_variant | MODIFIER | c.-4124C>T| |
S242 |
4 | BAA04g06230 | A04 | 4069050 | C | T | upstream_gene_variant | MODIFIER | c.-4113C>T| |
S246 |
5 | BAA04g06230 | A04 | 4069060 | G | A | upstream_gene_variant | MODIFIER | c.-4103G>A| |
S40 S49 |
6 | BAA04g06230 | A04 | 4069068 | C | T | upstream_gene_variant | MODIFIER | c.-4095C>T| |
S140 |
7 | BAA04g06230 | A04 | 4070868 | G | A | upstream_gene_variant | MODIFIER | c.-2295G>A| |
S197 |
8 | BAA04g06230 | A04 | 4071736 | C | T | upstream_gene_variant | MODIFIER | c.-1427C>T| |
S148 S210 |
9 | BAA04g06230 | A04 | 4072271 | C | T | upstream_gene_variant | MODIFIER | c.-892C>T| |
S260 |
10 | BAA04g06230 | A04 | 4074011 | G | A | missense_variant | MODERATE | c.533G>A|p.Gly178Glu |
S94 |
11 | BAA04g06230 | A04 | 4074932 | C | T | missense_variant | MODERATE | c.1454C>T|p.Thr485Ile |
S1 S90 |
12 | BAA04g06230 | A04 | 4075636 | C | T | missense_variant | MODERATE | c.2158C>T|p.Pro720Ser |
S192 |
13 | BAA04g06230 | A04 | 4076079 | G | A | downstream_gene_variant | MODIFIER | c.*426G>A| |
S57 |
14 | BAA04g06230 | A04 | 4076133 | G | A | downstream_gene_variant | MODIFIER | c.*480G>A| |
S114 |
15 | BAA04g06230 | A04 | 4076164 | G | A | downstream_gene_variant | MODIFIER | c.*511G>A| |
S50 |
16 | BAA04g06230 | A04 | 4076374 | C | T | downstream_gene_variant | MODIFIER | c.*721C>T| |
S193 |
17 | BAA04g06230 | A04 | 4076802 | G | A | downstream_gene_variant | MODIFIER | c.*1149G>A| |
S266 |
18 | BAA04g06230 | A04 | 4077336 | G | A | downstream_gene_variant | MODIFIER | c.*1683G>A| |
S205 |
19 | BAA04g06230 | A04 | 4077465 | G | A | downstream_gene_variant | MODIFIER | c.*1812G>A| |
S162 |