Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g01710 | A04 | 994093 | C | T | downstream_gene_variant | MODIFIER | c.*3844G>A| |
S82 S92 |
2 | BAA04g01710 | A04 | 994217 | G | A | downstream_gene_variant | MODIFIER | c.*3720C>T| |
S261 |
3 | BAA04g01710 | A04 | 994545 | C | T | downstream_gene_variant | MODIFIER | c.*3392G>A| |
S136 |
4 | BAA04g01710 | A04 | 995866 | C | T | downstream_gene_variant | MODIFIER | c.*2071G>A| |
S242 |
5 | BAA04g01710 | A04 | 998821 | C | T | synonymous_variant | LOW | c.468G>A|p.Thr156Thr |
S45 |
6 | BAA04g01710 | A04 | 998832 | G | A | missense_variant | MODERATE | c.457C>T|p.Leu153Phe |
S123 |
7 | BAA04g01710 | A04 | 998932 | C | T | synonymous_variant | LOW | c.357G>A|p.Glu119Glu |
S107 |
8 | BAA04g01710 | A04 | 999056 | G | A | missense_variant | MODERATE | c.233C>T|p.Ala78Val |
S153 S213 |
9 | BAA04g01710 | A04 | 999062 | C | T | missense_variant | MODERATE | c.227G>A|p.Gly76Glu |
S165 S211 |
10 | BAA04g01710 | A04 | 999318 | G | A | upstream_gene_variant | MODIFIER | c.-30C>T| |
S85 |
11 | BAA04g01710 | A04 | 1000437 | C | T | upstream_gene_variant | MODIFIER | c.-1149G>A| |
S208 S93 |
12 | BAA04g01710 | A04 | 1003752 | G | A | upstream_gene_variant | MODIFIER | c.-4464C>T| |
S57 |
13 | BAA04g01710 | A04 | 1003887 | C | T | upstream_gene_variant | MODIFIER | c.-4599G>A| |
S26 |
14 | BAA04g01710 | A04 | 1004242 | G | A | upstream_gene_variant | MODIFIER | c.-4954C>T| |
S75 S81 |