| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 69151 | BAA01g36180 | A01 | 24252584 | C | T | upstream_gene_variant | MODIFIER | c.-4430G>A| |
S112 |
| 69152 | BAA01g36190 | A01 | 24255771 | C | T | upstream_gene_variant | MODIFIER | c.-307C>T| |
S269 |
| 69153 | BAA01g36190 | A01 | 24256150 | C | T | missense_variant | MODERATE | c.73C>T|p.Pro25Ser |
S118 |
| 69154 | BAA01g36190 | A01 | 24256323 | C | T | synonymous_variant | LOW | c.246C>T|p.Tyr82Tyr |
S69 |
| 69155 | BAA01g36190 | A01 | 24256463 | G | A | missense_variant | MODERATE | c.386G>A|p.Arg129Lys |
S267 |
| 69156 | BAA01g36190 | A01 | 24256574 | G | A | missense_variant | MODERATE | c.497G>A|p.Gly166Glu |
S45 |
| 69157 | BAA01g36190 | A01 | 24256708 | G | A | missense_variant | MODERATE | c.631G>A|p.Glu211Lys |
S260 |
| 69158 | BAA01g36190 | A01 | 24256850 | C | T | missense_variant | MODERATE | c.773C>T|p.Ala258Val |
S12 |
| 69159 | BAA01g36190 | A01 | 24257112 | G | A | synonymous_variant | LOW | c.1035G>A|p.Leu345Leu |
S297 |
| 69160 | BAA01g36200 | A01 | 24257849 | G | A | upstream_gene_variant | MODIFIER | c.-4499G>A| |
S70 |
| 69161 | BAA01g36200 | A01 | 24258784 | G | A | upstream_gene_variant | MODIFIER | c.-3564G>A| |
S70 |
| 69162 | BAA01g36200 | A01 | 24259438 | C | T | upstream_gene_variant | MODIFIER | c.-2910C>T| |
S250 |
| 69163 | BAA01g36200 | A01 | 24259439 | G | A | upstream_gene_variant | MODIFIER | c.-2909G>A| |
S198 |
| 69164 | BAA01g36200 | A01 | 24259584 | C | T | upstream_gene_variant | MODIFIER | c.-2764C>T| |
S230 |
| 69165 | BAA01g36200 | A01 | 24260258 | G | A | upstream_gene_variant | MODIFIER | c.-2090G>A| |
S271 |
| 69166 | BAA01g36200 | A01 | 24260430 | C | T | upstream_gene_variant | MODIFIER | c.-1918C>T| |
S274 |
| 69167 | BAA01g36200 | A01 | 24260826 | G | A | upstream_gene_variant | MODIFIER | c.-1522G>A| |
S132 S137 S138 S215 S89 |
| 69168 | BAA01g36200 | A01 | 24261871 | A | T | upstream_gene_variant | MODIFIER | c.-477A>T| |
S47 |
| 69169 | BAA01g36200 | A01 | 24261872 | T | A | upstream_gene_variant | MODIFIER | c.-476T>A| |
S259 |
| 69170 | BAA01g36200 | A01 | 24262304 | G | A | upstream_gene_variant | MODIFIER | c.-44G>A| |
S109 |
| 69171 | BAA01g36200 | A01 | 24262456 | G | A | missense_variant | MODERATE | c.109G>A|p.Asp37Asn |
S114 |
| 69172 | BAA01g36200 | A01 | 24262676 | C | T | missense_variant | MODERATE | c.329C>T|p.Pro110Leu |
S19 |
| 69173 | BAA01g36200 | A01 | 24263090 | C | T | downstream_gene_variant | MODIFIER | c.*89C>T| |
S51 |
| 69174 | BAA01g36200 | A01 | 24263447 | G | A | downstream_gene_variant | MODIFIER | c.*446G>A| |
S71 |
| 69175 | BAA01g36200 | A01 | 24263499 | G | A | downstream_gene_variant | MODIFIER | c.*498G>A| |
S109 |