Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g26000 | A08 | 18597569 | G | A | upstream_gene_variant | MODIFIER | c.-3579G>A| |
S139 |
2 | BAA08g26000 | A08 | 18598007 | A | T | upstream_gene_variant | MODIFIER | c.-3141A>T| |
S292 |
3 | BAA08g26000 | A08 | 18599213 | G | A | upstream_gene_variant | MODIFIER | c.-1935G>A| |
S251 |
4 | BAA08g26000 | A08 | 18599446 | G | A | upstream_gene_variant | MODIFIER | c.-1702G>A| |
S202 |
5 | BAA08g26000 | A08 | 18600769 | G | A | upstream_gene_variant | MODIFIER | c.-379G>A| |
S68 |
6 | BAA08g26000 | A08 | 18600876 | C | T | upstream_gene_variant | MODIFIER | c.-272C>T| |
S299 |
7 | BAA08g26000 | A08 | 18601354 | G | A | synonymous_variant | LOW | c.207G>A|p.Glu69Glu |
S176 |
8 | BAA08g26000 | A08 | 18602386 | G | A | missense_variant | MODERATE | c.827G>A|p.Cys276Tyr |
S305 |
9 | BAA08g26000 | A08 | 18603696 | C | T | missense_variant | MODERATE | c.1549C>T|p.Pro517Ser |
S208 S219 |
10 | BAA08g26000 | A08 | 18604102 | G | A | missense_variant | MODERATE | c.1756G>A|p.Ala586Thr |
S195 S61 |
11 | BAA08g26000 | A08 | 18605047 | C | T | downstream_gene_variant | MODIFIER | c.*934C>T| |
S7 |
12 | BAA08g26000 | A08 | 18606546 | G | A | downstream_gene_variant | MODIFIER | c.*2433G>A| |
S54 |
13 | BAA08g26000 | A08 | 18607818 | C | T | downstream_gene_variant | MODIFIER | c.*3705C>T| |
S237 |