Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g44980 | A03 | 21412991 | C | T | downstream_gene_variant | MODIFIER | c.*3117G>A| |
S221 |
2 | BAA03g44980 | A03 | 21413033 | G | A | downstream_gene_variant | MODIFIER | c.*3075C>T| |
S45 |
3 | BAA03g44980 | A03 | 21413719 | C | T | downstream_gene_variant | MODIFIER | c.*2389G>A| |
S131 |
4 | BAA03g44980 | A03 | 21414037 | G | A | downstream_gene_variant | MODIFIER | c.*2071C>T| |
S6 |
5 | BAA03g44980 | A03 | 21414282 | G | A | downstream_gene_variant | MODIFIER | c.*1826C>T| |
S155 |
6 | BAA03g44980 | A03 | 21414427 | G | A | downstream_gene_variant | MODIFIER | c.*1681C>T| |
S56 |
7 | BAA03g44980 | A03 | 21414718 | A | G | downstream_gene_variant | MODIFIER | c.*1390T>C| |
S138 |
8 | BAA03g44980 | A03 | 21416124 | G | A | missense_variant | MODERATE | c.356C>T|p.Ser119Phe |
S34 |
9 | BAA03g44980 | A03 | 21416265 | G | A | missense_variant | MODERATE | c.215C>T|p.Ala72Val |
S218 |
10 | BAA03g44980 | A03 | 21417734 | C | T | upstream_gene_variant | MODIFIER | c.-1058G>A| |
S208 S219 |
11 | BAA03g44980 | A03 | 21417937 | G | A | upstream_gene_variant | MODIFIER | c.-1261C>T| |
S6 |
12 | BAA03g44980 | A03 | 21419018 | G | A | upstream_gene_variant | MODIFIER | c.-2342C>T| |
S14 |
13 | BAA03g44980 | A03 | 21420065 | C | T | upstream_gene_variant | MODIFIER | c.-3389G>A| |
S159 S243 |
14 | BAA03g44980 | A03 | 21420373 | C | T | upstream_gene_variant | MODIFIER | c.-3697G>A| |
S105 S106 |
15 | BAA03g44980 | A03 | 21421025 | G | A | upstream_gene_variant | MODIFIER | c.-4349C>T| |
S178 |