Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g68850 | A09 | 61737667 | G | A | upstream_gene_variant | MODIFIER | c.-4439G>A| |
S226 |
2 | BAA09g68850 | A09 | 61738904 | G | A | upstream_gene_variant | MODIFIER | c.-3202G>A| |
S206 S26 |
3 | BAA09g68850 | A09 | 61739060 | C | T | upstream_gene_variant | MODIFIER | c.-3046C>T| |
S58 |
4 | BAA09g68850 | A09 | 61739843 | G | A | upstream_gene_variant | MODIFIER | c.-2263G>A| |
S167 |
5 | BAA09g68850 | A09 | 61741401 | G | A | upstream_gene_variant | MODIFIER | c.-705G>A| |
S15 S3 |
6 | BAA09g68850 | A09 | 61741520 | G | A | upstream_gene_variant | MODIFIER | c.-586G>A| |
S268 |
7 | BAA09g68850 | A09 | 61741706 | C | T | upstream_gene_variant | MODIFIER | c.-400C>T| |
S62 |
8 | BAA09g68850 | A09 | 61741892 | C | T | upstream_gene_variant | MODIFIER | c.-214C>T| |
S38 |
9 | BAA09g68850 | A09 | 61741936 | C | T | upstream_gene_variant | MODIFIER | c.-170C>T| |
S18 |
10 | BAA09g68850 | A09 | 61742737 | C | T | missense_variant | MODERATE | c.376C>T|p.Arg126Cys |
S136 |
11 | BAA09g68850 | A09 | 61743399 | G | A | missense_variant | MODERATE | c.973G>A|p.Ala325Thr |
S295 |
12 | BAA09g68850 | A09 | 61744548 | C | T | downstream_gene_variant | MODIFIER | c.*433C>T| |
S267 |
13 | BAA09g68850 | A09 | 61745337 | C | T | downstream_gene_variant | MODIFIER | c.*1222C>T| |
S279 |
14 | BAA09g68850 | A09 | 61745458 | C | T | downstream_gene_variant | MODIFIER | c.*1343C>T| |
S211 S227 |
15 | BAA09g68850 | A09 | 61745702 | G | A | downstream_gene_variant | MODIFIER | c.*1587G>A| |
S244 |