| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g06660 | A10 | 3523056 | G | A | upstream_gene_variant | MODIFIER | c.-2604G>A| |
S100 |
| 2 | BAA10g06660 | A10 | 3523506 | G | A | upstream_gene_variant | MODIFIER | c.-2154G>A| |
S55 |
| 3 | BAA10g06660 | A10 | 3527957 | G | A | missense_variant | MODERATE | c.958G>A|p.Ala320Thr |
S284 |
| 4 | BAA10g06660 | A10 | 3529189 | C | T | downstream_gene_variant | MODIFIER | c.*1200C>T| |
S6 |
| 5 | BAA10g06660 | A10 | 3529739 | G | A | downstream_gene_variant | MODIFIER | c.*1750G>A| |
S223 |
| 6 | BAA10g06660 | A10 | 3529755 | G | A | downstream_gene_variant | MODIFIER | c.*1766G>A| |
S140 |
| 7 | BAA10g06660 | A10 | 3530617 | C | T | downstream_gene_variant | MODIFIER | c.*2628C>T| |
S237 |
| 8 | BAA10g06660 | A10 | 3530954 | C | T | downstream_gene_variant | MODIFIER | c.*2965C>T| |
S269 |
| 9 | BAA10g06660 | A10 | 3531866 | G | A | downstream_gene_variant | MODIFIER | c.*3877G>A| |
S230 |