Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g09980 | A09 | 5515976 | G | A | upstream_gene_variant | MODIFIER | c.-3372G>A| |
S16 |
2 | BAA09g09980 | A09 | 5516626 | C | T | upstream_gene_variant | MODIFIER | c.-2722C>T| |
S302 |
3 | BAA09g09980 | A09 | 5517396 | T | A | upstream_gene_variant | MODIFIER | c.-1952T>A| |
S155 |
4 | BAA09g09980 | A09 | 5517401 | C | T | upstream_gene_variant | MODIFIER | c.-1947C>T| |
S251 |
5 | BAA09g09980 | A09 | 5518593 | G | A | upstream_gene_variant | MODIFIER | c.-755G>A| |
S184 |
6 | BAA09g09980 | A09 | 5518738 | C | T | upstream_gene_variant | MODIFIER | c.-610C>T| |
S83 S88 |
7 | BAA09g09980 | A09 | 5518745 | G | A | upstream_gene_variant | MODIFIER | c.-603G>A| |
S174 S27 S39 |
8 | BAA09g09980 | A09 | 5518790 | C | T | upstream_gene_variant | MODIFIER | c.-558C>T| |
S69 |
9 | BAA09g09980 | A09 | 5518875 | G | A | upstream_gene_variant | MODIFIER | c.-473G>A| |
S162 |
10 | BAA09g09980 | A09 | 5519882 | C | T | missense_variant | MODERATE | c.376C>T|p.Leu126Phe |
S283 |
11 | BAA09g09980 | A09 | 5522390 | G | A | downstream_gene_variant | MODIFIER | c.*1876G>A| |
S115 |
12 | BAA09g09980 | A09 | 5524242 | C | T | downstream_gene_variant | MODIFIER | c.*3728C>T| |
S2 |
13 | BAA09g09980 | A09 | 5524432 | G | A | downstream_gene_variant | MODIFIER | c.*3918G>A| |
S308 |