Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g24840 | A10 | 20321941 | G | A | upstream_gene_variant | MODIFIER | c.-4904G>A| |
S286 |
2 | BAA10g24840 | A10 | 20321987 | C | T | upstream_gene_variant | MODIFIER | c.-4858C>T| |
S155 |
3 | BAA10g24840 | A10 | 20322081 | C | A | upstream_gene_variant | MODIFIER | c.-4764C>A| |
S305 |
4 | BAA10g24840 | A10 | 20322481 | C | T | upstream_gene_variant | MODIFIER | c.-4364C>T| |
S202 |
5 | BAA10g24840 | A10 | 20322744 | G | A | upstream_gene_variant | MODIFIER | c.-4101G>A| |
S53 |
6 | BAA10g24840 | A10 | 20324579 | C | T | upstream_gene_variant | MODIFIER | c.-2266C>T| |
S170 |
7 | BAA10g24840 | A10 | 20324925 | C | T | upstream_gene_variant | MODIFIER | c.-1920C>T| |
S292 |
8 | BAA10g24840 | A10 | 20326177 | G | A | upstream_gene_variant | MODIFIER | c.-668G>A| |
S295 |
9 | BAA10g24840 | A10 | 20327173 | C | T | missense_variant | MODERATE | c.329C>T|p.Ser110Leu |
S185 |
10 | BAA10g24840 | A10 | 20327497 | C | T | missense_variant | MODERATE | c.653C>T|p.Thr218Ile |
S161 |