Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g22260 | A02 | 12024574 | C | T | upstream_gene_variant | MODIFIER | c.-3431C>T| |
S144 |
2 | BAA02g22260 | A02 | 12025418 | G | A | upstream_gene_variant | MODIFIER | c.-2587G>A| |
S272 |
3 | BAA02g22260 | A02 | 12026436 | C | T | upstream_gene_variant | MODIFIER | c.-1569C>T| |
S293 |
4 | BAA02g22260 | A02 | 12026652 | C | T | upstream_gene_variant | MODIFIER | c.-1353C>T| |
S80 |
5 | BAA02g22260 | A02 | 12027504 | G | A | upstream_gene_variant | MODIFIER | c.-501G>A| |
S199 |
6 | BAA02g22260 | A02 | 12028231 | G | A | missense_variant | MODERATE | c.227G>A|p.Gly76Asp |
S58 |
7 | BAA02g22260 | A02 | 12028233 | C | T | missense_variant | MODERATE | c.229C>T|p.Pro77Ser |
S261 |
8 | BAA02g22260 | A02 | 12028517 | C | A | synonymous_variant | LOW | c.513C>A|p.Ala171Ala |
S94 |
9 | BAA02g22260 | A02 | 12028782 | G | A | missense_variant | MODERATE | c.778G>A|p.Glu260Lys |
S192 |
10 | BAA02g22260 | A02 | 12028947 | G | A | missense_variant | MODERATE | c.943G>A|p.Asp315Asn |
S149 |
11 | BAA02g22260 | A02 | 12030070 | G | A | downstream_gene_variant | MODIFIER | c.*337G>A| |
S132 S215 |
12 | BAA02g22260 | A02 | 12030458 | C | T | downstream_gene_variant | MODIFIER | c.*725C>T| |
S205 |
13 | BAA02g22260 | A02 | 12031481 | G | A | downstream_gene_variant | MODIFIER | c.*1748G>A| |
S247 |
14 | BAA02g22260 | A02 | 12032935 | C | T | downstream_gene_variant | MODIFIER | c.*3202C>T| |
S267 |
15 | BAA02g22260 | A02 | 12033131 | C | T | downstream_gene_variant | MODIFIER | c.*3398C>T| |
S80 |
16 | BAA02g22260 | A02 | 12033240 | C | T | downstream_gene_variant | MODIFIER | c.*3507C>T| |
S221 |