Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g13190 | A02 | 5973370 | C | T | downstream_gene_variant | MODIFIER | c.*4974G>A| |
S87 |
2 | BAA02g13190 | A02 | 5973919 | G | A | downstream_gene_variant | MODIFIER | c.*4425C>T| |
S109 |
3 | BAA02g13190 | A02 | 5976477 | C | T | downstream_gene_variant | MODIFIER | c.*1867G>A| |
S174 |
4 | BAA02g13190 | A02 | 5976785 | C | T | downstream_gene_variant | MODIFIER | c.*1559G>A| |
S47 |
5 | BAA02g13190 | A02 | 5977111 | G | A | downstream_gene_variant | MODIFIER | c.*1233C>T| |
S17 |
6 | BAA02g13190 | A02 | 5977207 | C | T | downstream_gene_variant | MODIFIER | c.*1137G>A| |
S240 |
7 | BAA02g13190 | A02 | 5978453 | G | A | missense_variant | MODERATE | c.230C>T|p.Thr77Ile |
S59 |
8 | BAA02g13190 | A02 | 5979778 | C | T | upstream_gene_variant | MODIFIER | c.-1096G>A| |
S38 |
9 | BAA02g13190 | A02 | 5981351 | C | T | upstream_gene_variant | MODIFIER | c.-2669G>A| |
S249 |