Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g54400 | A09 | 55066549 | C | T | downstream_gene_variant | MODIFIER | c.*3132G>A| |
S152 |
2 | BAA09g54400 | A09 | 55067820 | G | A | downstream_gene_variant | MODIFIER | c.*1861C>T| |
S172 S217 |
3 | BAA09g54400 | A09 | 55068475 | C | T | downstream_gene_variant | MODIFIER | c.*1206G>A| |
S81 S85 |
4 | BAA09g54400 | A09 | 55068707 | G | A | downstream_gene_variant | MODIFIER | c.*974C>T| |
S143 |
5 | BAA09g54400 | A09 | 55069292 | C | T | downstream_gene_variant | MODIFIER | c.*389G>A| |
S154 S67 |
6 | BAA09g54400 | A09 | 55070063 | G | A | missense_variant | MODERATE | c.1409C>T|p.Thr470Ile |
S113 |
7 | BAA09g54400 | A09 | 55070264 | C | T | missense_variant | MODERATE | c.1208G>A|p.Gly403Asp |
S138 |
8 | BAA09g54400 | A09 | 55070564 | G | A | missense_variant | MODERATE | c.908C>T|p.Ala303Val |
S162 |
9 | BAA09g54400 | A09 | 55070666 | C | T | missense_variant | MODERATE | c.806G>A|p.Arg269Lys |
S125 |
10 | BAA09g54400 | A09 | 55072286 | C | T | upstream_gene_variant | MODIFIER | c.-639G>A| |
S236 |
11 | BAA09g54400 | A09 | 55075335 | G | A | upstream_gene_variant | MODIFIER | c.-3688C>T| |
S270 |
12 | BAA09g54400 | A09 | 55075770 | G | A | upstream_gene_variant | MODIFIER | c.-4123C>T| |
S243 |
13 | BAA09g54400 | A09 | 55076260 | C | T | upstream_gene_variant | MODIFIER | c.-4613G>A| |
S293 |