Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g27000 | A09 | 17536705 | G | A | upstream_gene_variant | MODIFIER | c.-4363G>A| |
S126 |
2 | BAA09g27000 | A09 | 17536963 | C | T | upstream_gene_variant | MODIFIER | c.-4105C>T| |
S195 |
3 | BAA09g27000 | A09 | 17537698 | C | T | upstream_gene_variant | MODIFIER | c.-3370C>T| |
S2 |
4 | BAA09g27000 | A09 | 17537946 | C | T | upstream_gene_variant | MODIFIER | c.-3122C>T| |
S212 |
5 | BAA09g27000 | A09 | 17541135 | G | A | missense_variant | MODERATE | c.68G>A|p.Gly23Asp |
S237 |
6 | BAA09g27000 | A09 | 17541292 | G | A | missense_variant | MODERATE | c.133G>A|p.Val45Ile |
S42 |
7 | BAA09g27000 | A09 | 17541425 | T | A | missense_variant | MODERATE | c.266T>A|p.Ile89Lys |
S186 |
8 | BAA09g27000 | A09 | 17541519 | G | A | stop_gained | HIGH | c.360G>A|p.Trp120* |
S267 |
9 | BAA09g27000 | A09 | 17541663 | G | A | missense_variant | MODERATE | c.409G>A|p.Ala137Thr |
S295 |
10 | BAA09g27000 | A09 | 17541725 | C | T | synonymous_variant | LOW | c.471C>T|p.Arg157Arg |
S139 |
11 | BAA09g27000 | A09 | 17541901 | C | T | downstream_gene_variant | MODIFIER | c.*89C>T| |
S282 |