Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g35960 | A09 | 44296794 | C | T | downstream_gene_variant | MODIFIER | c.*4235G>A| |
S36 |
2 | BAA09g35960 | A09 | 44297766 | C | T | downstream_gene_variant | MODIFIER | c.*3263G>A| |
S193 |
3 | BAA09g35960 | A09 | 44298126 | G | A | downstream_gene_variant | MODIFIER | c.*2903C>T| |
S210 S225 |
4 | BAA09g35960 | A09 | 44298280 | C | T | downstream_gene_variant | MODIFIER | c.*2749G>A| |
S286 |
5 | BAA09g35960 | A09 | 44298442 | G | A | downstream_gene_variant | MODIFIER | c.*2587C>T| |
S209 |
6 | BAA09g35960 | A09 | 44299164 | G | A | downstream_gene_variant | MODIFIER | c.*1865C>T| |
S98 |
7 | BAA09g35960 | A09 | 44299444 | C | T | downstream_gene_variant | MODIFIER | c.*1585G>A| |
S135 |
8 | BAA09g35960 | A09 | 44299730 | C | T | downstream_gene_variant | MODIFIER | c.*1299G>A| |
S224 |
9 | BAA09g35960 | A09 | 44301173 | C | T | synonymous_variant | LOW | c.1317G>A|p.Lys439Lys |
S136 |
10 | BAA09g35960 | A09 | 44301686 | C | T | missense_variant | MODERATE | c.979G>A|p.Ala327Thr |
S113 |
11 | BAA09g35960 | A09 | 44305506 | C | T | upstream_gene_variant | MODIFIER | c.-2151G>A| |
S153 |
12 | BAA09g35960 | A09 | 44305702 | C | T | upstream_gene_variant | MODIFIER | c.-2347G>A| |
S53 |
13 | BAA09g35960 | A09 | 44306327 | C | T | upstream_gene_variant | MODIFIER | c.-2972G>A| |
S183 |