| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g08950 | A10 | 10990345 | C | T | downstream_gene_variant | MODIFIER | c.*4664G>A| |
S114 |
| 2 | BAA10g08950 | A10 | 10991312 | C | T | downstream_gene_variant | MODIFIER | c.*3697G>A| |
S281 |
| 3 | BAA10g08950 | A10 | 10991605 | G | A | downstream_gene_variant | MODIFIER | c.*3404C>T| |
S55 |
| 4 | BAA10g08950 | A10 | 10992117 | T | C | downstream_gene_variant | MODIFIER | c.*2892A>G| |
S240 |
| 5 | BAA10g08950 | A10 | 10992237 | G | A | downstream_gene_variant | MODIFIER | c.*2772C>T| |
S129 |
| 6 | BAA10g08950 | A10 | 10992254 | C | T | downstream_gene_variant | MODIFIER | c.*2755G>A| |
S144 S189 |
| 7 | BAA10g08950 | A10 | 10992306 | G | A | downstream_gene_variant | MODIFIER | c.*2703C>T| |
S245 |
| 8 | BAA10g08950 | A10 | 10995626 | G | A | intron_variant | MODIFIER | c.579+92C>T| |
S251 |
| 9 | BAA10g08950 | A10 | 10996688 | C | T | intron_variant | MODIFIER | c.47-31G>A| |
S157 |
| 10 | BAA10g08950 | A10 | 10996807 | C | T | stop_gained | HIGH | c.24G>A|p.Trp8* |
S42 |
| 11 | BAA10g08950 | A10 | 10998491 | C | T | upstream_gene_variant | MODIFIER | c.-1661G>A| |
S173 |
| 12 | BAA10g08950 | A10 | 10999897 | G | A | upstream_gene_variant | MODIFIER | c.-3067C>T| |
S15 S3 |
| 13 | BAA10g08950 | A10 | 11000814 | C | T | upstream_gene_variant | MODIFIER | c.-3984G>A| |
S270 |
| 14 | BAA10g08950 | A10 | 11000991 | C | T | upstream_gene_variant | MODIFIER | c.-4161G>A| |
S142 |
| 15 | BAA10g08950 | A10 | 11001640 | G | A | upstream_gene_variant | MODIFIER | c.-4810C>T| |
S283 |