Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g09660 | A10 | 11578129 | C | T | downstream_gene_variant | MODIFIER | c.*3822G>A| |
S259 |
2 | BAA10g09660 | A10 | 11579094 | G | A | downstream_gene_variant | MODIFIER | c.*2857C>T| |
S289 |
3 | BAA10g09660 | A10 | 11580832 | C | T | downstream_gene_variant | MODIFIER | c.*1119G>A| |
S259 |
4 | BAA10g09660 | A10 | 11584194 | C | T | missense_variant | MODERATE | c.226G>A|p.Ala76Thr |
S204 |
5 | BAA10g09660 | A10 | 11585301 | G | A | upstream_gene_variant | MODIFIER | c.-600C>T| |
S13 S140 S279 S64 |
6 | BAA10g09660 | A10 | 11586604 | C | T | upstream_gene_variant | MODIFIER | c.-1903G>A| |
S165 |
7 | BAA10g09660 | A10 | 11587125 | G | A | upstream_gene_variant | MODIFIER | c.-2424C>T| |
S261 |
8 | BAA10g09660 | A10 | 11587186 | G | A | upstream_gene_variant | MODIFIER | c.-2485C>T| |
S68 |
9 | BAA10g09660 | A10 | 11589550 | C | T | upstream_gene_variant | MODIFIER | c.-4849G>A| |
S5 |