Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g41930 | A02 | 35012591 | G | A | upstream_gene_variant | MODIFIER | c.-4426G>A| |
S148 S210 |
2 | BAA02g41930 | A02 | 35012790 | G | A | upstream_gene_variant | MODIFIER | c.-4227G>A| |
S282 |
3 | BAA02g41930 | A02 | 35012796 | C | T | upstream_gene_variant | MODIFIER | c.-4221C>T| |
S122 |
4 | BAA02g41930 | A02 | 35013121 | C | T | upstream_gene_variant | MODIFIER | c.-3896C>T| |
S160 |
5 | BAA02g41930 | A02 | 35013526 | G | A | upstream_gene_variant | MODIFIER | c.-3491G>A| |
S125 |
6 | BAA02g41930 | A02 | 35013796 | G | A | upstream_gene_variant | MODIFIER | c.-3221G>A| |
S50 |
7 | BAA02g41930 | A02 | 35014617 | G | A | upstream_gene_variant | MODIFIER | c.-2400G>A| |
S287 |
8 | BAA02g41930 | A02 | 35015133 | G | A | upstream_gene_variant | MODIFIER | c.-1884G>A| |
S306 |
9 | BAA02g41930 | A02 | 35018228 | C | T | synonymous_variant | LOW | c.511C>T|p.Leu171Leu |
S139 |
10 | BAA02g41930 | A02 | 35019239 | C | T | synonymous_variant | LOW | c.1026C>T|p.Asp342Asp |
S42 |
11 | BAA02g41930 | A02 | 35019292 | G | A | missense_variant | MODERATE | c.1079G>A|p.Arg360Lys |
S176 |
12 | BAA02g41930 | A02 | 35020225 | C | T | synonymous_variant | LOW | c.1671C>T|p.Ser557Ser |
S244 |
13 | BAA02g41930 | A02 | 35022414 | G | A | downstream_gene_variant | MODIFIER | c.*1846G>A| |
S207 |
14 | BAA02g41930 | A02 | 35025187 | C | T | downstream_gene_variant | MODIFIER | c.*4619C>T| |
S124 |