Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g07250 | A02 | 3112566 | C | T | upstream_gene_variant | MODIFIER | c.-4339C>T| |
S167 |
2 | BAA02g07250 | A02 | 3112639 | G | A | upstream_gene_variant | MODIFIER | c.-4266G>A| |
S96 |
3 | BAA02g07250 | A02 | 3113470 | C | T | upstream_gene_variant | MODIFIER | c.-3435C>T| |
S87 |
4 | BAA02g07250 | A02 | 3113574 | C | T | upstream_gene_variant | MODIFIER | c.-3331C>T| |
S167 |
5 | BAA02g07250 | A02 | 3117193 | G | A | missense_variant | MODERATE | c.289G>A|p.Gly97Arg |
S144 |
6 | BAA02g07250 | A02 | 3117232 | G | A | missense_variant | MODERATE | c.328G>A|p.Val110Met |
S64 |
7 | BAA02g07250 | A02 | 3117546 | G | A | synonymous_variant | LOW | c.642G>A|p.Lys214Lys |
S45 |
8 | BAA02g07250 | A02 | 3119755 | G | A | missense_variant | MODERATE | c.1727G>A|p.Gly576Asp |
S166 |
9 | BAA02g07250 | A02 | 3120205 | G | A | missense_variant | MODERATE | c.2177G>A|p.Gly726Asp |
S9 |
10 | BAA02g07250 | A02 | 3120423 | G | A | missense_variant | MODERATE | c.2395G>A|p.Ala799Thr |
S37 |
11 | BAA02g07250 | A02 | 3124847 | G | A | downstream_gene_variant | MODIFIER | c.*3396G>A| |
S9 |
12 | BAA02g07250 | A02 | 3124965 | C | T | downstream_gene_variant | MODIFIER | c.*3514C>T| |
S218 |