Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g26170 | A05 | 30865800 | G | A | upstream_gene_variant | MODIFIER | c.-4602G>A| |
S265 |
2 | BAA05g26170 | A05 | 30866678 | C | T | upstream_gene_variant | MODIFIER | c.-3724C>T| |
S100 |
3 | BAA05g26170 | A05 | 30867751 | C | T | upstream_gene_variant | MODIFIER | c.-2651C>T| |
S208 |
4 | BAA05g26170 | A05 | 30868394 | G | A | upstream_gene_variant | MODIFIER | c.-2008G>A| |
S282 |
5 | BAA05g26170 | A05 | 30868934 | T | A | upstream_gene_variant | MODIFIER | c.-1468T>A| |
S273 |
6 | BAA05g26170 | A05 | 30869306 | G | A | upstream_gene_variant | MODIFIER | c.-1096G>A| |
S178 |
7 | BAA05g26170 | A05 | 30869548 | G | A | upstream_gene_variant | MODIFIER | c.-854G>A| |
S218 |
8 | BAA05g26170 | A05 | 30870275 | C | T | upstream_gene_variant | MODIFIER | c.-127C>T| |
S123 |
9 | BAA05g26170 | A05 | 30870328 | G | A | upstream_gene_variant | MODIFIER | c.-74G>A| |
S228 |
10 | BAA05g26170 | A05 | 30870523 | G | A | missense_variant | MODERATE | c.122G>A|p.Gly41Glu |
S110 |
11 | BAA05g26170 | A05 | 30870699 | G | A | missense_variant | MODERATE | c.298G>A|p.Gly100Ser |
S166 |
12 | BAA05g26170 | A05 | 30873497 | C | T | downstream_gene_variant | MODIFIER | c.*2778C>T| |
S27 |
13 | BAA05g26170 | A05 | 30873625 | G | A | downstream_gene_variant | MODIFIER | c.*2906G>A| |
S51 |
14 | BAA05g26170 | A05 | 30874318 | G | A | downstream_gene_variant | MODIFIER | c.*3599G>A| |
S23 |