| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g08840 | A10 | 10842183 | C | T | downstream_gene_variant | MODIFIER | c.*2427G>A| |
S301 S304 |
| 2 | BAA10g08840 | A10 | 10843527 | G | A | downstream_gene_variant | MODIFIER | c.*1083C>T| |
S181 |
| 3 | BAA10g08840 | A10 | 10843822 | C | T | downstream_gene_variant | MODIFIER | c.*788G>A| |
S193 |
| 4 | BAA10g08840 | A10 | 10843834 | T | C | downstream_gene_variant | MODIFIER | c.*776A>G| |
S128 |
| 5 | BAA10g08840 | A10 | 10843875 | C | T | downstream_gene_variant | MODIFIER | c.*735G>A| |
S186 |
| 6 | BAA10g08840 | A10 | 10844552 | G | A | downstream_gene_variant | MODIFIER | c.*58C>T| |
S13 |
| 7 | BAA10g08840 | A10 | 10845072 | C | T | synonymous_variant | LOW | c.1731G>A|p.Gln577Gln |
S10 |
| 8 | BAA10g08840 | A10 | 10845315 | C | T | synonymous_variant | LOW | c.1488G>A|p.Pro496Pro |
S92 |
| 9 | BAA10g08840 | A10 | 10846203 | G | A | synonymous_variant | LOW | c.600C>T|p.Ile200Ile |
S274 |
| 10 | BAA10g08840 | A10 | 10846547 | G | A | missense_variant | MODERATE | c.256C>T|p.Arg86Trp |
S209 |
| 11 | BAA10g08840 | A10 | 10847801 | G | A | upstream_gene_variant | MODIFIER | c.-999C>T| |
S176 |
| 12 | BAA10g08840 | A10 | 10848189 | C | T | upstream_gene_variant | MODIFIER | c.-1387G>A| |
S133 |
| 13 | BAA10g08840 | A10 | 10848968 | C | T | upstream_gene_variant | MODIFIER | c.-2166G>A| |
S144 |
| 14 | BAA10g08840 | A10 | 10849717 | G | A | upstream_gene_variant | MODIFIER | c.-2915C>T| |
S35 |
| 15 | BAA10g08840 | A10 | 10850172 | C | T | upstream_gene_variant | MODIFIER | c.-3370G>A| |
S297 |
| 16 | BAA10g08840 | A10 | 10850960 | G | A | upstream_gene_variant | MODIFIER | c.-4158C>T| |
S278 |
| 17 | BAA10g08840 | A10 | 10850962 | G | A | upstream_gene_variant | MODIFIER | c.-4160C>T| |
S209 |