Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g11270 | A02 | 5082864 | G | A | missense_variant | MODERATE | c.526C>T|p.His176Tyr |
S139 |
2 | BAA02g11270 | A02 | 5083851 | G | A | upstream_gene_variant | MODIFIER | c.-274C>T| |
S295 |
3 | BAA02g11270 | A02 | 5084394 | G | A | upstream_gene_variant | MODIFIER | c.-817C>T| |
S150 |
4 | BAA02g11270 | A02 | 5086490 | G | A | upstream_gene_variant | MODIFIER | c.-2913C>T| |
S247 |
5 | BAA02g11270 | A02 | 5086855 | G | A | upstream_gene_variant | MODIFIER | c.-3278C>T| |
S298 |