Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g17740 | A10 | 16916080 | G | A | missense_variant | MODERATE | c.326C>T|p.Thr109Met |
S202 |
2 | BAA10g17740 | A10 | 16916114 | T | C | missense_variant | MODERATE | c.292A>G|p.Ser98Gly |
S128 |
3 | BAA10g17740 | A10 | 16917260 | C | T | upstream_gene_variant | MODIFIER | c.-855G>A| |
S25 |
4 | BAA10g17740 | A10 | 16917509 | C | T | upstream_gene_variant | MODIFIER | c.-1104G>A| |
S153 S213 |
5 | BAA10g17740 | A10 | 16918205 | C | T | upstream_gene_variant | MODIFIER | c.-1800G>A| |
S259 |
6 | BAA10g17740 | A10 | 16918382 | C | T | upstream_gene_variant | MODIFIER | c.-1977G>A| |
S308 |
7 | BAA10g17740 | A10 | 16919404 | G | A | upstream_gene_variant | MODIFIER | c.-2999C>T| |
S16 |
8 | BAA10g17740 | A10 | 16919421 | G | A | upstream_gene_variant | MODIFIER | c.-3016C>T| |
S136 |
9 | BAA10g17740 | A10 | 16920705 | G | A | upstream_gene_variant | MODIFIER | c.-4300C>T| |
S252 |
10 | BAA10g17740 | A10 | 16920844 | C | T | upstream_gene_variant | MODIFIER | c.-4439G>A| |
S152 |
11 | BAA10g17740 | A10 | 16921230 | C | T | upstream_gene_variant | MODIFIER | c.-4825G>A| |
S156 |