| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g11190 | A10 | 12826462 | C | T | downstream_gene_variant | MODIFIER | c.*3016G>A| |
S247 |
| 2 | BAA10g11190 | A10 | 12827379 | C | T | downstream_gene_variant | MODIFIER | c.*2099G>A| |
S297 |
| 3 | BAA10g11190 | A10 | 12829530 | G | A | missense_variant | MODERATE | c.665C>T|p.Ala222Val |
S18 |
| 4 | BAA10g11190 | A10 | 12829813 | G | A | splice_region_variant&intron_variant | LOW | c.572-7C>T| |
S283 |
| 5 | BAA10g11190 | A10 | 12830279 | T | G | missense_variant | MODERATE | c.149A>C|p.Asn50Thr |
S179 S204 S301 S303 S43 S78 |
| 6 | BAA10g11190 | A10 | 12830339 | C | T | missense_variant | MODERATE | c.89G>A|p.Arg30Lys |
S176 |
| 7 | BAA10g11190 | A10 | 12830551 | G | A | upstream_gene_variant | MODIFIER | c.-124C>T| |
S18 |
| 8 | BAA10g11190 | A10 | 12831090 | G | A | upstream_gene_variant | MODIFIER | c.-663C>T| |
S262 |
| 9 | BAA10g11190 | A10 | 12831633 | G | A | upstream_gene_variant | MODIFIER | c.-1206C>T| |
S45 |
| 10 | BAA10g11190 | A10 | 12833524 | C | T | upstream_gene_variant | MODIFIER | c.-3097G>A| |
S42 |