Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g27640 | A08 | 19402107 | G | A | upstream_gene_variant | MODIFIER | c.-4667G>A| |
S273 |
2 | BAA08g27640 | A08 | 19402350 | C | T | upstream_gene_variant | MODIFIER | c.-4424C>T| |
S274 |
3 | BAA08g27640 | A08 | 19403086 | C | T | upstream_gene_variant | MODIFIER | c.-3688C>T| |
S180 |
4 | BAA08g27640 | A08 | 19403160 | C | T | upstream_gene_variant | MODIFIER | c.-3614C>T| |
S13 |
5 | BAA08g27640 | A08 | 19403340 | C | T | upstream_gene_variant | MODIFIER | c.-3434C>T| |
S208 |
6 | BAA08g27640 | A08 | 19406837 | G | A | missense_variant | MODERATE | c.64G>A|p.Val22Ile |
S117 |
7 | BAA08g27640 | A08 | 19407021 | C | T | missense_variant | MODERATE | c.248C>T|p.Ser83Phe |
S178 |
8 | BAA08g27640 | A08 | 19407136 | C | T | synonymous_variant | LOW | c.363C>T|p.Phe121Phe |
S105 S106 |
9 | BAA08g27640 | A08 | 19407266 | C | T | missense_variant | MODERATE | c.493C>T|p.Pro165Ser |
S19 |
10 | BAA08g27640 | A08 | 19407639 | G | A | missense_variant | MODERATE | c.866G>A|p.Gly289Glu |
S221 |
11 | BAA08g27640 | A08 | 19408110 | G | A | missense_variant | MODERATE | c.1178G>A|p.Arg393Gln |
S260 |
12 | BAA08g27640 | A08 | 19408166 | G | A | missense_variant | MODERATE | c.1234G>A|p.Ala412Thr |
S190 |
13 | BAA08g27640 | A08 | 19410456 | G | A | downstream_gene_variant | MODIFIER | c.*2249G>A| |
S265 |
14 | BAA08g27640 | A08 | 19411646 | C | T | downstream_gene_variant | MODIFIER | c.*3439C>T| |
S230 |
15 | BAA08g27640 | A08 | 19411680 | G | A | downstream_gene_variant | MODIFIER | c.*3473G>A| |
S265 |
16 | BAA08g27640 | A08 | 19412144 | C | T | downstream_gene_variant | MODIFIER | c.*3937C>T| |
S255 |
17 | BAA08g27640 | A08 | 19412418 | G | T | downstream_gene_variant | MODIFIER | c.*4211G>T| |
S139 S184 S198 S200 S221 S41 |