| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g03910 | A10 | 1910204 | C | T | upstream_gene_variant | MODIFIER | c.-4800C>T| |
S84 S93 |
| 2 | BAA10g03910 | A10 | 1910226 | G | A | upstream_gene_variant | MODIFIER | c.-4778G>A| |
S138 |
| 3 | BAA10g03910 | A10 | 1910260 | C | T | upstream_gene_variant | MODIFIER | c.-4744C>T| |
S225 |
| 4 | BAA10g03910 | A10 | 1911423 | C | T | upstream_gene_variant | MODIFIER | c.-3581C>T| |
S23 |
| 5 | BAA10g03910 | A10 | 1911523 | C | T | upstream_gene_variant | MODIFIER | c.-3481C>T| |
S305 |
| 6 | BAA10g03910 | A10 | 1915331 | C | T | missense_variant | MODERATE | c.116C>T|p.Ala39Val |
S87 |
| 7 | BAA10g03910 | A10 | 1915348 | C | T | missense_variant | MODERATE | c.133C>T|p.Arg45Trp |
S197 |
| 8 | BAA10g03910 | A10 | 1917460 | G | A | splice_region_variant&synonymous_variant | LOW | c.489G>A|p.Gly163Gly |
S178 |
| 9 | BAA10g03910 | A10 | 1919664 | C | T | missense_variant | MODERATE | c.842C>T|p.Thr281Ile |
S123 |