Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g29810 | A02 | 17137949 | G | A | downstream_gene_variant | MODIFIER | c.*4258C>T| |
S256 |
2 | BAA02g29810 | A02 | 17138083 | G | T | downstream_gene_variant | MODIFIER | c.*4124C>A| |
S178 |
3 | BAA02g29810 | A02 | 17138260 | G | A | downstream_gene_variant | MODIFIER | c.*3947C>T| |
S53 |
4 | BAA02g29810 | A02 | 17138312 | G | A | downstream_gene_variant | MODIFIER | c.*3895C>T| |
S150 |
5 | BAA02g29810 | A02 | 17139067 | C | T | downstream_gene_variant | MODIFIER | c.*3140G>A| |
S167 |
6 | BAA02g29810 | A02 | 17139086 | G | A | downstream_gene_variant | MODIFIER | c.*3121C>T| |
S209 |
7 | BAA02g29810 | A02 | 17139295 | G | A | downstream_gene_variant | MODIFIER | c.*2912C>T| |
S256 |
8 | BAA02g29810 | A02 | 17140299 | G | A | downstream_gene_variant | MODIFIER | c.*1908C>T| |
S245 S246 |
9 | BAA02g29810 | A02 | 17141476 | G | A | downstream_gene_variant | MODIFIER | c.*731C>T| |
S278 |
10 | BAA02g29810 | A02 | 17141703 | G | A | downstream_gene_variant | MODIFIER | c.*504C>T| |
S148 S30 S31 |
11 | BAA02g29810 | A02 | 17141824 | C | T | downstream_gene_variant | MODIFIER | c.*383G>A| |
S224 |
12 | BAA02g29810 | A02 | 17142292 | C | T | missense_variant | MODERATE | c.122G>A|p.Gly41Asp |
S73 S91 |
13 | BAA02g29810 | A02 | 17142856 | G | A | upstream_gene_variant | MODIFIER | c.-443C>T| |
S113 |
14 | BAA02g29810 | A02 | 17144453 | C | T | upstream_gene_variant | MODIFIER | c.-2040G>A| |
S167 |
15 | BAA02g29810 | A02 | 17145187 | C | T | upstream_gene_variant | MODIFIER | c.-2774G>A| |
S15 S156 S3 S34 |
16 | BAA02g29810 | A02 | 17145514 | G | A | upstream_gene_variant | MODIFIER | c.-3101C>T| |
S281 |
17 | BAA02g29810 | A02 | 17146101 | C | T | upstream_gene_variant | MODIFIER | c.-3688G>A| |
S167 |
18 | BAA02g29810 | A02 | 17147238 | G | A | upstream_gene_variant | MODIFIER | c.-4825C>T| |
S265 |