Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g34620 | A02 | 29700743 | G | A | downstream_gene_variant | MODIFIER | c.*4571C>T| |
S176 |
2 | BAA02g34620 | A02 | 29702534 | C | T | downstream_gene_variant | MODIFIER | c.*2780G>A| |
S33 |
3 | BAA02g34620 | A02 | 29702585 | C | T | downstream_gene_variant | MODIFIER | c.*2729G>A| |
S78 S83 |
4 | BAA02g34620 | A02 | 29702784 | C | T | downstream_gene_variant | MODIFIER | c.*2530G>A| |
S112 |
5 | BAA02g34620 | A02 | 29705461 | G | A | synonymous_variant | LOW | c.1011C>T|p.Tyr337Tyr |
S268 |
6 | BAA02g34620 | A02 | 29706430 | C | T | missense_variant | MODERATE | c.916G>A|p.Ala306Thr |
S179 |
7 | BAA02g34620 | A02 | 29706624 | G | A | missense_variant | MODERATE | c.845C>T|p.Ser282Phe |
S99 |
8 | BAA02g34620 | A02 | 29706874 | G | A | missense_variant | MODERATE | c.683C>T|p.Thr228Met |
S71 |
9 | BAA02g34620 | A02 | 29708074 | G | A | missense_variant | MODERATE | c.23C>T|p.Ser8Phe |
S146 |
10 | BAA02g34620 | A02 | 29708345 | G | A | upstream_gene_variant | MODIFIER | c.-249C>T| |
S247 |
11 | BAA02g34620 | A02 | 29708958 | C | T | upstream_gene_variant | MODIFIER | c.-862G>A| |
S234 |
12 | BAA02g34620 | A02 | 29709699 | C | T | upstream_gene_variant | MODIFIER | c.-1603G>A| |
S46 |
13 | BAA02g34620 | A02 | 29710695 | G | A | upstream_gene_variant | MODIFIER | c.-2599C>T| |
S279 |
14 | BAA02g34620 | A02 | 29711337 | G | A | upstream_gene_variant | MODIFIER | c.-3241C>T| |
S197 |
15 | BAA02g34620 | A02 | 29712220 | C | T | upstream_gene_variant | MODIFIER | c.-4124G>A| |
S87 |
16 | BAA02g34620 | A02 | 29712227 | G | A | upstream_gene_variant | MODIFIER | c.-4131C>T| |
S294 |
17 | BAA02g34620 | A02 | 29712255 | C | T | upstream_gene_variant | MODIFIER | c.-4159G>A| |
S6 |
18 | BAA02g34620 | A02 | 29712655 | G | A | upstream_gene_variant | MODIFIER | c.-4559C>T| |
S256 |