Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g35960 | A08 | 22745791 | G | A | upstream_gene_variant | MODIFIER | c.-4256G>A| |
S107 |
2 | BAA08g35960 | A08 | 22745853 | C | T | upstream_gene_variant | MODIFIER | c.-4194C>T| |
S178 |
3 | BAA08g35960 | A08 | 22746743 | G | A | upstream_gene_variant | MODIFIER | c.-3304G>A| |
S55 |
4 | BAA08g35960 | A08 | 22747092 | G | A | upstream_gene_variant | MODIFIER | c.-2955G>A| |
S165 |
5 | BAA08g35960 | A08 | 22747104 | G | A | upstream_gene_variant | MODIFIER | c.-2943G>A| |
S162 |
6 | BAA08g35960 | A08 | 22747476 | C | T | upstream_gene_variant | MODIFIER | c.-2571C>T| |
S69 |
7 | BAA08g35960 | A08 | 22747940 | G | A | upstream_gene_variant | MODIFIER | c.-2107G>A| |
S275 |
8 | BAA08g35960 | A08 | 22748332 | C | T | upstream_gene_variant | MODIFIER | c.-1715C>T| |
S210 S225 |
9 | BAA08g35960 | A08 | 22750066 | C | T | missense_variant | MODERATE | c.20C>T|p.Thr7Ile |
S177 |
10 | BAA08g35960 | A08 | 22750460 | C | T | synonymous_variant | LOW | c.414C>T|p.Pro138Pro |
S284 |
11 | BAA08g35960 | A08 | 22750645 | G | A | downstream_gene_variant | MODIFIER | c.*53G>A| |
S209 |
12 | BAA08g35960 | A08 | 22753132 | C | T | downstream_gene_variant | MODIFIER | c.*2540C>T| |
S201 |
13 | BAA08g35960 | A08 | 22753724 | G | A | downstream_gene_variant | MODIFIER | c.*3132G>A| |
S39 |
14 | BAA08g35960 | A08 | 22754134 | G | A | downstream_gene_variant | MODIFIER | c.*3542G>A| |
S216 |