Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g07030 | A02 | 3004017 | C | T | upstream_gene_variant | MODIFIER | c.-3195C>T| |
S257 |
2 | BAA02g07030 | A02 | 3004210 | G | A | upstream_gene_variant | MODIFIER | c.-3002G>A| |
S143 |
3 | BAA02g07030 | A02 | 3004247 | G | A | upstream_gene_variant | MODIFIER | c.-2965G>A| |
S61 |
4 | BAA02g07030 | A02 | 3004760 | C | T | upstream_gene_variant | MODIFIER | c.-2452C>T| |
S277 |
5 | BAA02g07030 | A02 | 3005225 | C | T | upstream_gene_variant | MODIFIER | c.-1987C>T| |
S19 |
6 | BAA02g07030 | A02 | 3005589 | G | A | upstream_gene_variant | MODIFIER | c.-1623G>A| |
S288 |
7 | BAA02g07030 | A02 | 3005853 | G | A | upstream_gene_variant | MODIFIER | c.-1359G>A| |
S61 |
8 | BAA02g07030 | A02 | 3006064 | G | A | upstream_gene_variant | MODIFIER | c.-1148G>A| |
S139 |
9 | BAA02g07030 | A02 | 3007291 | C | T | missense_variant | MODERATE | c.80C>T|p.Ser27Phe |
S240 |
10 | BAA02g07030 | A02 | 3007349 | G | A | stop_gained | HIGH | c.138G>A|p.Trp46* |
S110 |
11 | BAA02g07030 | A02 | 3007454 | C | T | synonymous_variant | LOW | c.243C>T|p.Ile81Ile |
S123 |
12 | BAA02g07030 | A02 | 3008475 | C | T | intron_variant | MODIFIER | c.1249+15C>T| |
S230 |
13 | BAA02g07030 | A02 | 3008494 | G | A | intron_variant | MODIFIER | c.1249+34G>A| |
S89 |
14 | BAA02g07030 | A02 | 3010274 | G | A | downstream_gene_variant | MODIFIER | c.*941G>A| |
S237 |
15 | BAA02g07030 | A02 | 3011352 | G | A | downstream_gene_variant | MODIFIER | c.*2019G>A| |
S187 |
16 | BAA02g07030 | A02 | 3011462 | C | T | downstream_gene_variant | MODIFIER | c.*2129C>T| |
S18 |
17 | BAA02g07030 | A02 | 3012211 | G | A | downstream_gene_variant | MODIFIER | c.*2878G>A| |
S158 |