Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g21400 | A02 | 11489877 | G | A | downstream_gene_variant | MODIFIER | c.*1529C>T| |
S264 |
2 | BAA02g21400 | A02 | 11490248 | G | A | downstream_gene_variant | MODIFIER | c.*1158C>T| |
S159 S243 |
3 | BAA02g21400 | A02 | 11490459 | C | T | downstream_gene_variant | MODIFIER | c.*947G>A| |
S108 |
4 | BAA02g21400 | A02 | 11491022 | G | A | downstream_gene_variant | MODIFIER | c.*384C>T| |
S286 |
5 | BAA02g21400 | A02 | 11491108 | C | T | downstream_gene_variant | MODIFIER | c.*298G>A| |
S6 |
6 | BAA02g21400 | A02 | 11491608 | C | T | missense_variant | MODERATE | c.1721G>A|p.Cys574Tyr |
S115 |
7 | BAA02g21400 | A02 | 11492269 | C | T | missense_variant | MODERATE | c.1228G>A|p.Gly410Arg |
S124 |
8 | BAA02g21400 | A02 | 11493664 | G | A | missense_variant | MODERATE | c.289C>T|p.Leu97Phe |
S116 |
9 | BAA02g21400 | A02 | 11494150 | G | A | upstream_gene_variant | MODIFIER | c.-198C>T| |
S161 |
10 | BAA02g21400 | A02 | 11495067 | G | A | upstream_gene_variant | MODIFIER | c.-1115C>T| |
S306 S308 |
11 | BAA02g21400 | A02 | 11497220 | C | T | upstream_gene_variant | MODIFIER | c.-3268G>A| |
S202 |
12 | BAA02g21400 | A02 | 11497494 | G | A | upstream_gene_variant | MODIFIER | c.-3542C>T| |
S69 |
13 | BAA02g21400 | A02 | 11498328 | C | T | upstream_gene_variant | MODIFIER | c.-4376G>A| |
S163 |