Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g20280 | A05 | 12418560 | C | T | upstream_gene_variant | MODIFIER | c.-4872C>T| |
S266 |
2 | BAA05g20280 | A05 | 12419261 | C | T | upstream_gene_variant | MODIFIER | c.-4171C>T| |
S85 |
3 | BAA05g20280 | A05 | 12419262 | C | T | upstream_gene_variant | MODIFIER | c.-4170C>T| |
S233 |
4 | BAA05g20280 | A05 | 12419415 | C | T | upstream_gene_variant | MODIFIER | c.-4017C>T| |
S211 S227 |
5 | BAA05g20280 | A05 | 12419714 | C | T | upstream_gene_variant | MODIFIER | c.-3718C>T| |
S164 |
6 | BAA05g20280 | A05 | 12420042 | C | T | upstream_gene_variant | MODIFIER | c.-3390C>T| |
S287 |
7 | BAA05g20280 | A05 | 12420193 | G | A | upstream_gene_variant | MODIFIER | c.-3239G>A| |
S192 |
8 | BAA05g20280 | A05 | 12423189 | C | T | upstream_gene_variant | MODIFIER | c.-243C>T| |
S195 |
9 | BAA05g20280 | A05 | 12423435 | G | A | missense_variant | MODERATE | c.4G>A|p.Val2Met |
S150 |
10 | BAA05g20280 | A05 | 12423495 | G | A | missense_variant | MODERATE | c.64G>A|p.Ala22Thr |
S261 |
11 | BAA05g20280 | A05 | 12424624 | G | A | downstream_gene_variant | MODIFIER | c.*1001G>A| |
S103 |
12 | BAA05g20280 | A05 | 12424752 | G | A | downstream_gene_variant | MODIFIER | c.*1129G>A| |
S55 |
13 | BAA05g20280 | A05 | 12425055 | G | A | downstream_gene_variant | MODIFIER | c.*1432G>A| |
S291 |
14 | BAA05g20280 | A05 | 12425126 | G | A | downstream_gene_variant | MODIFIER | c.*1503G>A| |
S54 |
15 | BAA05g20280 | A05 | 12425425 | G | A | downstream_gene_variant | MODIFIER | c.*1802G>A| |
S226 |
16 | BAA05g20280 | A05 | 12425775 | C | T | downstream_gene_variant | MODIFIER | c.*2152C>T| |
S58 |
17 | BAA05g20280 | A05 | 12426913 | G | A | downstream_gene_variant | MODIFIER | c.*3290G>A| |
S68 |
18 | BAA05g20280 | A05 | 12427068 | G | A | downstream_gene_variant | MODIFIER | c.*3445G>A| |
S272 |
19 | BAA05g20280 | A05 | 12427599 | C | T | downstream_gene_variant | MODIFIER | c.*3976C>T| |
S69 |
20 | BAA05g20280 | A05 | 12427707 | G | A | downstream_gene_variant | MODIFIER | c.*4084G>A| |
S152 |