Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g47660 | A02 | 38425029 | G | A | downstream_gene_variant | MODIFIER | c.*4642C>T| |
S30 |
2 | BAA02g47660 | A02 | 38426700 | C | T | downstream_gene_variant | MODIFIER | c.*2971G>A| |
S299 |
3 | BAA02g47660 | A02 | 38428703 | C | T | downstream_gene_variant | MODIFIER | c.*968G>A| |
S250 |
4 | BAA02g47660 | A02 | 38429212 | G | A | downstream_gene_variant | MODIFIER | c.*459C>T| |
S286 |
5 | BAA02g47660 | A02 | 38429387 | C | T | downstream_gene_variant | MODIFIER | c.*284G>A| |
S15 S3 |
6 | BAA02g47660 | A02 | 38429795 | G | A | missense_variant | MODERATE | c.1289C>T|p.Ser430Phe |
S200 |
7 | BAA02g47660 | A02 | 38429861 | C | T | missense_variant | MODERATE | c.1223G>A|p.Cys408Tyr |
S171 |
8 | BAA02g47660 | A02 | 38430103 | C | T | synonymous_variant | LOW | c.981G>A|p.Glu327Glu |
S296 |
9 | BAA02g47660 | A02 | 38430235 | C | T | synonymous_variant | LOW | c.849G>A|p.Ala283Ala |
S112 |
10 | BAA02g47660 | A02 | 38430486 | G | A | missense_variant | MODERATE | c.598C>T|p.Pro200Ser |
S143 |
11 | BAA02g47660 | A02 | 38432467 | C | T | upstream_gene_variant | MODIFIER | c.-1162G>A| |
S211 |
12 | BAA02g47660 | A02 | 38432821 | C | T | upstream_gene_variant | MODIFIER | c.-1516G>A| |
S262 |
13 | BAA02g47660 | A02 | 38433264 | C | T | upstream_gene_variant | MODIFIER | c.-1959G>A| |
S183 S198 |
14 | BAA02g47660 | A02 | 38433918 | C | T | upstream_gene_variant | MODIFIER | c.-2613G>A| |
S18 |
15 | BAA02g47660 | A02 | 38434734 | G | A | upstream_gene_variant | MODIFIER | c.-3429C>T| |
S185 |
16 | BAA02g47660 | A02 | 38435715 | C | T | upstream_gene_variant | MODIFIER | c.-4410G>A| |
S18 |