| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 116051 | BAA10g10130 | A10 | 11879066 | C | T | upstream_gene_variant | MODIFIER | c.-254C>T| |
S199 |
| 116052 | BAA10g10140 | A10 | 11879761 | C | T | upstream_gene_variant | MODIFIER | c.-3188C>T| |
S244 |
| 116053 | BAA10g10140 | A10 | 11879959 | G | A | upstream_gene_variant | MODIFIER | c.-2990G>A| |
S148 S30 S31 |
| 116054 | BAA10g10140 | A10 | 11880323 | T | G | upstream_gene_variant | MODIFIER | c.-2626T>G| |
S99 |
| 116055 | BAA10g10140 | A10 | 11880771 | C | T | upstream_gene_variant | MODIFIER | c.-2178C>T| |
S37 |
| 116056 | BAA10g10140 | A10 | 11880804 | G | A | upstream_gene_variant | MODIFIER | c.-2145G>A| |
S240 |
| 116057 | BAA10g10140 | A10 | 11881169 | G | A | upstream_gene_variant | MODIFIER | c.-1780G>A| |
S140 |
| 116058 | BAA10g10140 | A10 | 11881731 | C | T | upstream_gene_variant | MODIFIER | c.-1218C>T| |
S152 |
| 116059 | BAA10g10140 | A10 | 11882849 | C | T | upstream_gene_variant | MODIFIER | c.-100C>T| |
S297 |
| 116060 | BAA10g10140 | A10 | 11884076 | G | A | synonymous_variant | LOW | c.1128G>A|p.Arg376Arg |
S107 |
| 116061 | BAA10g10140 | A10 | 11884555 | C | T | missense_variant | MODERATE | c.1607C>T|p.Ser536Phe |
S224 |
| 116062 | BAA10g10140 | A10 | 11885420 | C | T | downstream_gene_variant | MODIFIER | c.*144C>T| |
S166 |
| 116063 | BAA10g10140 | A10 | 11885776 | G | A | downstream_gene_variant | MODIFIER | c.*500G>A| |
S64 |
| 116064 | BAA10g10140 | A10 | 11886171 | C | T | downstream_gene_variant | MODIFIER | c.*895C>T| |
S305 |
| 116065 | BAA10g10140 | A10 | 11886430 | C | T | downstream_gene_variant | MODIFIER | c.*1154C>T| |
S166 |
| 116066 | BAA10g10140 | A10 | 11886450 | G | A | downstream_gene_variant | MODIFIER | c.*1174G>A| |
S111 |
| 116067 | BAA10g10140 | A10 | 11887058 | G | A | downstream_gene_variant | MODIFIER | c.*1782G>A| |
S160 |
| 116068 | BAA10g10140 | A10 | 11888357 | G | A | downstream_gene_variant | MODIFIER | c.*3081G>A| |
S198 |
| 116069 | BAA10g10140-BAA10g10150 | A10 | 11890758 | G | A | intergenic_region | MODIFIER | n.11890758G>A| |
S221 |
| 116070 | BAA10g10140-BAA10g10150 | A10 | 11892154 | C | T | intergenic_region | MODIFIER | n.11892154C>T| |
S54 |
| 116071 | BAA10g10140-BAA10g10150 | A10 | 11892561 | C | T | intergenic_region | MODIFIER | n.11892561C>T| |
S297 |
| 116072 | BAA10g10140-BAA10g10150 | A10 | 11892587 | G | A | intergenic_region | MODIFIER | n.11892587G>A| |
S125 |
| 116073 | BAA10g10140-BAA10g10150 | A10 | 11893115 | C | T | intergenic_region | MODIFIER | n.11893115C>T| |
S243 S299 |
| 116074 | BAA10g10140-BAA10g10150 | A10 | 11893237 | G | A | intergenic_region | MODIFIER | n.11893237G>A| |
S217 S248 |
| 116075 | BAA10g10140-BAA10g10150 | A10 | 11894711 | G | A | intergenic_region | MODIFIER | n.11894711G>A| |
S90 |