Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g18130 | A02 | 9116949 | C | T | downstream_gene_variant | MODIFIER | c.*1899G>A| |
S8 |
2 | BAA02g18130 | A02 | 9117941 | G | A | downstream_gene_variant | MODIFIER | c.*907C>T| |
S247 |
3 | BAA02g18130 | A02 | 9119373 | G | A | missense_variant | MODERATE | c.719C>T|p.Pro240Leu |
S280 |
4 | BAA02g18130 | A02 | 9120174 | G | A | missense_variant | MODERATE | c.241C>T|p.Pro81Ser |
S150 |
5 | BAA02g18130 | A02 | 9120970 | C | T | upstream_gene_variant | MODIFIER | c.-165G>A| |
S128 |
6 | BAA02g18130 | A02 | 9121018 | G | A | upstream_gene_variant | MODIFIER | c.-213C>T| |
S259 |
7 | BAA02g18130 | A02 | 9121594 | C | T | upstream_gene_variant | MODIFIER | c.-789G>A| |
S123 |
8 | BAA02g18130 | A02 | 9121818 | G | A | upstream_gene_variant | MODIFIER | c.-1013C>T| |
S23 |
9 | BAA02g18130 | A02 | 9124190 | C | T | upstream_gene_variant | MODIFIER | c.-3385G>A| |
S5 |
10 | BAA02g18130 | A02 | 9124861 | C | T | upstream_gene_variant | MODIFIER | c.-4056G>A| |
S255 |
11 | BAA02g18130 | A02 | 9124925 | C | T | upstream_gene_variant | MODIFIER | c.-4120G>A| |
S301 S304 |
12 | BAA02g18130 | A02 | 9125572 | C | T | upstream_gene_variant | MODIFIER | c.-4767G>A| |
S230 |
13 | BAA02g18130 | A02 | 9125710 | C | T | upstream_gene_variant | MODIFIER | c.-4905G>A| |
S175 |