| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g11900 | A10 | 13455038 | C | T | upstream_gene_variant | MODIFIER | c.-3622C>T| |
S87 |
| 2 | BAA10g11900 | A10 | 13455882 | G | A | upstream_gene_variant | MODIFIER | c.-2778G>A| |
S264 |
| 3 | BAA10g11900 | A10 | 13457516 | G | A | upstream_gene_variant | MODIFIER | c.-1144G>A| |
S279 |
| 4 | BAA10g11900 | A10 | 13457696 | C | T | upstream_gene_variant | MODIFIER | c.-964C>T| |
S298 |
| 5 | BAA10g11900 | A10 | 13458396 | G | A | upstream_gene_variant | MODIFIER | c.-264G>A| |
S274 |
| 6 | BAA10g11900 | A10 | 13459462 | C | T | missense_variant | MODERATE | c.803C>T|p.Ser268Phe |
S44 |
| 7 | BAA10g11900 | A10 | 13460549 | G | A | missense_variant | MODERATE | c.1890G>A|p.Met630Ile |
S296 |
| 8 | BAA10g11900 | A10 | 13461119 | G | A | stop_gained | HIGH | c.2460G>A|p.Trp820* |
S148 S210 S30 S31 |
| 9 | BAA10g11900 | A10 | 13461125 | G | A | synonymous_variant | LOW | c.2466G>A|p.Val822Val |
S207 |
| 10 | BAA10g11900 | A10 | 13461341 | G | A | synonymous_variant | LOW | c.2682G>A|p.Pro894Pro |
S48 |
| 11 | BAA10g11900 | A10 | 13463077 | C | T | downstream_gene_variant | MODIFIER | c.*1415C>T| |
S180 |
| 12 | BAA10g11900 | A10 | 13463305 | C | T | downstream_gene_variant | MODIFIER | c.*1643C>T| |
S68 |
| 13 | BAA10g11900 | A10 | 13464097 | C | T | downstream_gene_variant | MODIFIER | c.*2435C>T| |
S96 |
| 14 | BAA10g11900 | A10 | 13464794 | C | A | downstream_gene_variant | MODIFIER | c.*3132C>A| |
S13 S140 S219 S279 S64 S72 |
| 15 | BAA10g11900 | A10 | 13465700 | G | A | downstream_gene_variant | MODIFIER | c.*4038G>A| |
S66 |
| 16 | BAA10g11900 | A10 | 13465926 | C | T | downstream_gene_variant | MODIFIER | c.*4264C>T| |
S242 |
| 17 | BAA10g11900 | A10 | 13465962 | C | T | downstream_gene_variant | MODIFIER | c.*4300C>T| |
S294 |