| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA06g32610 | A06 | 22067243 | C | T | downstream_gene_variant | MODIFIER | c.*4452G>A| |
S247 |
| 2 | BAA06g32610 | A06 | 22067332 | G | A | downstream_gene_variant | MODIFIER | c.*4363C>T| |
S165 |
| 3 | BAA06g32610 | A06 | 22067480 | G | A | downstream_gene_variant | MODIFIER | c.*4215C>T| |
S54 |
| 4 | BAA06g32610 | A06 | 22067708 | G | A | downstream_gene_variant | MODIFIER | c.*3987C>T| |
S19 |
| 5 | BAA06g32610 | A06 | 22067822 | C | T | downstream_gene_variant | MODIFIER | c.*3873G>A| |
S133 S192 |
| 6 | BAA06g32610 | A06 | 22070629 | G | A | downstream_gene_variant | MODIFIER | c.*1066C>T| |
S90 |
| 7 | BAA06g32610 | A06 | 22074041 | C | T | synonymous_variant | LOW | c.1143G>A|p.Gly381Gly |
S84 S93 |
| 8 | BAA06g32610 | A06 | 22074043 | C | T | missense_variant | MODERATE | c.1141G>A|p.Gly381Arg |
S6 |
| 9 | BAA06g32610 | A06 | 22075213 | G | A | missense_variant | MODERATE | c.560C>T|p.Ala187Val |
S168 |
| 10 | BAA06g32610 | A06 | 22076069 | C | T | intron_variant | MODIFIER | c.317+207G>A| |
S96 |
| 11 | BAA06g32610 | A06 | 22076872 | C | T | upstream_gene_variant | MODIFIER | c.-101G>A| |
S295 |
| 12 | BAA06g32610 | A06 | 22077855 | G | A | upstream_gene_variant | MODIFIER | c.-1084C>T| |
S66 |
| 13 | BAA06g32610 | A06 | 22077993 | G | A | upstream_gene_variant | MODIFIER | c.-1222C>T| |
S131 |
| 14 | BAA06g32610 | A06 | 22078084 | C | T | upstream_gene_variant | MODIFIER | c.-1313G>A| |
S117 |
| 15 | BAA06g32610 | A06 | 22078837 | G | A | upstream_gene_variant | MODIFIER | c.-2066C>T| |
S138 |
| 16 | BAA06g32610 | A06 | 22080776 | G | A | upstream_gene_variant | MODIFIER | c.-4005C>T| |
S20 |
| 17 | BAA06g32610 | A06 | 22081428 | G | A | upstream_gene_variant | MODIFIER | c.-4657C>T| |
S268 |