Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g19020 | A02 | 9831223 | G | A | upstream_gene_variant | MODIFIER | c.-4418G>A| |
S5 |
2 | BAA02g19020 | A02 | 9831751 | C | T | upstream_gene_variant | MODIFIER | c.-3890C>T| |
S75 S81 |
3 | BAA02g19020 | A02 | 9832430 | C | A | upstream_gene_variant | MODIFIER | c.-3211C>A| |
S136 S202 S53 |
4 | BAA02g19020 | A02 | 9834319 | G | A | upstream_gene_variant | MODIFIER | c.-1322G>A| |
S162 |
5 | BAA02g19020 | A02 | 9834491 | C | T | upstream_gene_variant | MODIFIER | c.-1150C>T| |
S221 |
6 | BAA02g19020 | A02 | 9837180 | C | T | intron_variant | MODIFIER | c.379+1161C>T| |
S277 |
7 | BAA02g19020 | A02 | 9838610 | G | A | intron_variant | MODIFIER | c.380-95G>A| |
S70 |
8 | BAA02g19020 | A02 | 9838936 | C | T | missense_variant | MODERATE | c.611C>T|p.Ser204Phe |
S202 |
9 | BAA02g19020 | A02 | 9839137 | G | A | synonymous_variant | LOW | c.714G>A|p.Thr238Thr |
S158 |
10 | BAA02g19020 | A02 | 9839491 | G | A | missense_variant | MODERATE | c.980G>A|p.Arg327Lys |
S129 |
11 | BAA02g19020 | A02 | 9841499 | C | T | synonymous_variant | LOW | c.2253C>T|p.Ile751Ile |
S103 |
12 | BAA02g19020 | A02 | 9843182 | C | T | downstream_gene_variant | MODIFIER | c.*1194C>T| |
S104 S52 |
13 | BAA02g19020 | A02 | 9843348 | C | T | downstream_gene_variant | MODIFIER | c.*1360C>T| |
S42 |
14 | BAA02g19020 | A02 | 9843812 | G | A | downstream_gene_variant | MODIFIER | c.*1824G>A| |
S217 S248 |
15 | BAA02g19020 | A02 | 9843968 | C | T | downstream_gene_variant | MODIFIER | c.*1980C>T| |
S305 |