Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g09840 | A10 | 11697014 | G | A | upstream_gene_variant | MODIFIER | c.-4594G>A| |
S85 |
2 | BAA10g09840 | A10 | 11697256 | C | T | upstream_gene_variant | MODIFIER | c.-4352C>T| |
S19 |
3 | BAA10g09840 | A10 | 11697294 | C | T | upstream_gene_variant | MODIFIER | c.-4314C>T| |
S168 |
4 | BAA10g09840 | A10 | 11697396 | C | T | upstream_gene_variant | MODIFIER | c.-4212C>T| |
S249 S38 |
5 | BAA10g09840 | A10 | 11697682 | C | T | upstream_gene_variant | MODIFIER | c.-3926C>T| |
S162 |
6 | BAA10g09840 | A10 | 11697801 | C | T | upstream_gene_variant | MODIFIER | c.-3807C>T| |
S146 |
7 | BAA10g09840 | A10 | 11697888 | C | T | upstream_gene_variant | MODIFIER | c.-3720C>T| |
S19 |
8 | BAA10g09840 | A10 | 11698158 | C | T | upstream_gene_variant | MODIFIER | c.-3450C>T| |
S96 |
9 | BAA10g09840 | A10 | 11698660 | G | A | upstream_gene_variant | MODIFIER | c.-2948G>A| |
S88 |
10 | BAA10g09840 | A10 | 11698896 | G | A | upstream_gene_variant | MODIFIER | c.-2712G>A| |
S150 |
11 | BAA10g09840 | A10 | 11698960 | C | T | upstream_gene_variant | MODIFIER | c.-2648C>T| |
S225 S73 |
12 | BAA10g09840 | A10 | 11702162 | C | T | missense_variant | MODERATE | c.449C>T|p.Ala150Val |
S38 |