| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g26370 | A10 | 20943020 | C | T | downstream_gene_variant | MODIFIER | c.*901G>A| |
S148 S210 S30 S31 |
| 2 | BAA10g26370 | A10 | 20944090 | G | A | missense_variant | MODERATE | c.236C>T|p.Ala79Val |
S136 |
| 3 | BAA10g26370 | A10 | 20944266 | C | T | synonymous_variant | LOW | c.60G>A|p.Arg20Arg |
S210 S225 |
| 4 | BAA10g26370 | A10 | 20945440 | G | A | upstream_gene_variant | MODIFIER | c.-1115C>T| |
S270 |
| 5 | BAA10g26370 | A10 | 20946414 | G | A | upstream_gene_variant | MODIFIER | c.-2089C>T| |
S100 |
| 6 | BAA10g26370 | A10 | 20946468 | C | T | upstream_gene_variant | MODIFIER | c.-2143G>A| |
S162 |
| 7 | BAA10g26370 | A10 | 20947852 | C | T | upstream_gene_variant | MODIFIER | c.-3527G>A| |
S277 |
| 8 | BAA10g26370 | A10 | 20948393 | C | T | upstream_gene_variant | MODIFIER | c.-4068G>A| |
S168 |
| 9 | BAA10g26370 | A10 | 20949177 | C | T | upstream_gene_variant | MODIFIER | c.-4852G>A| |
S238 |