Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g24330 | A02 | 13281746 | G | A | upstream_gene_variant | MODIFIER | c.-4986G>A| |
S12 S17 |
2 | BAA02g24330 | A02 | 13281780 | G | A | upstream_gene_variant | MODIFIER | c.-4952G>A| |
S197 |
3 | BAA02g24330 | A02 | 13281801 | C | T | upstream_gene_variant | MODIFIER | c.-4931C>T| |
S283 |
4 | BAA02g24330 | A02 | 13282270 | G | A | upstream_gene_variant | MODIFIER | c.-4462G>A| |
S219 S72 |
5 | BAA02g24330 | A02 | 13284565 | C | T | upstream_gene_variant | MODIFIER | c.-2167C>T| |
S32 |
6 | BAA02g24330 | A02 | 13288132 | G | A | missense_variant | MODERATE | c.643G>A|p.Gly215Ser |
S156 |
7 | BAA02g24330 | A02 | 13288422 | C | T | missense_variant | MODERATE | c.802C>T|p.Pro268Ser |
S11 |
8 | BAA02g24330 | A02 | 13289345 | G | A | missense_variant | MODERATE | c.1204G>A|p.Val402Met |
S37 |
9 | BAA02g24330 | A02 | 13289638 | C | T | synonymous_variant | LOW | c.1419C>T|p.Asn473Asn |
S218 |
10 | BAA02g24330 | A02 | 13290080 | C | T | missense_variant | MODERATE | c.1771C>T|p.Leu591Phe |
S268 |
11 | BAA02g24330 | A02 | 13290751 | G | A | downstream_gene_variant | MODIFIER | c.*85G>A| |
S263 |
12 | BAA02g24330 | A02 | 13291182 | C | T | downstream_gene_variant | MODIFIER | c.*516C>T| |
S206 |
13 | BAA02g24330 | A02 | 13291684 | C | T | downstream_gene_variant | MODIFIER | c.*1018C>T| |
S2 |