Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g08140 | A02 | 3502505 | C | T | missense_variant | MODERATE | c.2782G>A|p.Val928Met |
S63 |
2 | BAA02g08140 | A02 | 3503127 | G | A | missense_variant | MODERATE | c.2242C>T|p.Leu748Phe |
S205 |
3 | BAA02g08140 | A02 | 3503560 | G | A | synonymous_variant | LOW | c.1809C>T|p.Phe603Phe |
S82 S92 |
4 | BAA02g08140 | A02 | 3503710 | G | A | synonymous_variant | LOW | c.1659C>T|p.Leu553Leu |
S4 |
5 | BAA02g08140 | A02 | 3504390 | C | T | missense_variant | MODERATE | c.979G>A|p.Glu327Lys |
S6 |
6 | BAA02g08140 | A02 | 3505230 | G | A | synonymous_variant | LOW | c.243C>T|p.Cys81Cys |
S84 S93 |
7 | BAA02g08140 | A02 | 3505692 | C | T | upstream_gene_variant | MODIFIER | c.-139G>A| |
S249 |
8 | BAA02g08140 | A02 | 3507412 | C | T | upstream_gene_variant | MODIFIER | c.-1859G>A| |
S46 |
9 | BAA02g08140 | A02 | 3508617 | C | T | upstream_gene_variant | MODIFIER | c.-3064G>A| |
S280 |
10 | BAA02g08140 | A02 | 3509571 | G | A | upstream_gene_variant | MODIFIER | c.-4018C>T| |
S198 |
11 | BAA02g08140 | A02 | 3509599 | G | A | upstream_gene_variant | MODIFIER | c.-4046C>T| |
S294 |