Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g12960 | A07 | 21062301 | G | A | downstream_gene_variant | MODIFIER | c.*461C>T| |
S157 S163 |
2 | BAA07g12960 | A07 | 21062438 | C | T | downstream_gene_variant | MODIFIER | c.*324G>A| |
S230 |
3 | BAA07g12960 | A07 | 21062661 | G | A | downstream_gene_variant | MODIFIER | c.*101C>T| |
S109 |
4 | BAA07g12960 | A07 | 21062702 | G | A | downstream_gene_variant | MODIFIER | c.*60C>T| |
S158 |
5 | BAA07g12960 | A07 | 21063818 | C | T | missense_variant | MODERATE | c.1100G>A|p.Arg367Gln |
S130 |
6 | BAA07g12960 | A07 | 21064082 | C | T | intron_variant | MODIFIER | c.857-21G>A| |
S118 |
7 | BAA07g12960 | A07 | 21064368 | C | T | intron_variant | MODIFIER | c.646-25G>A| |
S233 |
8 | BAA07g12960 | A07 | 21064428 | G | A | intron_variant | MODIFIER | c.646-85C>T| |
S269 |
9 | BAA07g12960 | A07 | 21066078 | C | T | upstream_gene_variant | MODIFIER | c.-866G>A| |
S216 |
10 | BAA07g12960 | A07 | 21066329 | C | T | upstream_gene_variant | MODIFIER | c.-1117G>A| |
S180 |
11 | BAA07g12960 | A07 | 21066990 | G | A | upstream_gene_variant | MODIFIER | c.-1778C>T| |
S175 |
12 | BAA07g12960 | A07 | 21068399 | C | T | upstream_gene_variant | MODIFIER | c.-3187G>A| |
S249 |
13 | BAA07g12960 | A07 | 21068921 | C | T | upstream_gene_variant | MODIFIER | c.-3709G>A| |
S4 |
14 | BAA07g12960 | A07 | 21069894 | G | A | upstream_gene_variant | MODIFIER | c.-4682C>T| |
S219 S284 S72 |
15 | BAA07g12960 | A07 | 21070132 | C | T | upstream_gene_variant | MODIFIER | c.-4920G>A| |
S306 S308 |