| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 183101 | BAA02g21840-BAA02g21850 | A02 | 11758867 | C | T | intergenic_region | MODIFIER | n.11758867C>T| |
S266 |
| 183102 | BAA02g21840-BAA02g21850 | A02 | 11759206 | A | T | intergenic_region | MODIFIER | n.11759206A>T| |
S185 |
| 183103 | BAA02g21840-BAA02g21850 | A02 | 11759371 | C | T | intergenic_region | MODIFIER | n.11759371C>T| |
S302 |
| 183104 | BAA02g21840-BAA02g21850 | A02 | 11759459 | C | T | intergenic_region | MODIFIER | n.11759459C>T| |
S262 |
| 183105 | BAA02g21850 | A02 | 11760413 | G | A | upstream_gene_variant | MODIFIER | c.-4442G>A| |
S174 S27 |
| 183106 | BAA02g21850 | A02 | 11760555 | G | A | upstream_gene_variant | MODIFIER | c.-4300G>A| |
S86 |
| 183107 | BAA02g21850 | A02 | 11760643 | G | A | upstream_gene_variant | MODIFIER | c.-4212G>A| |
S161 |
| 183108 | BAA02g21850 | A02 | 11760892 | C | T | upstream_gene_variant | MODIFIER | c.-3963C>T| |
S107 |
| 183109 | BAA02g21850 | A02 | 11761647 | C | T | upstream_gene_variant | MODIFIER | c.-3208C>T| |
S234 |
| 183110 | BAA02g21850 | A02 | 11762349 | G | T | upstream_gene_variant | MODIFIER | c.-2506G>T| |
S188 |
| 183111 | BAA02g21850 | A02 | 11762522 | C | T | upstream_gene_variant | MODIFIER | c.-2333C>T| |
S42 |
| 183112 | BAA02g21850 | A02 | 11762727 | C | T | upstream_gene_variant | MODIFIER | c.-2128C>T| |
S183 S198 |
| 183113 | BAA02g21850 | A02 | 11763997 | G | A | upstream_gene_variant | MODIFIER | c.-858G>A| |
S48 |
| 183114 | BAA02g21850 | A02 | 11764391 | C | T | upstream_gene_variant | MODIFIER | c.-464C>T| |
S224 |
| 183115 | BAA02g21850 | A02 | 11765349 | G | A | missense_variant | MODERATE | c.416G>A|p.Ser139Asn |
S68 |
| 183116 | BAA02g21850 | A02 | 11765861 | G | A | missense_variant | MODERATE | c.928G>A|p.Glu310Lys |
S126 |
| 183117 | BAA02g21850 | A02 | 11766958 | G | A | missense_variant | MODERATE | c.1739G>A|p.Arg580Lys |
S295 |
| 183118 | BAA02g21850 | A02 | 11767648 | G | A | missense_variant | MODERATE | c.2429G>A|p.Gly810Glu |
S278 |
| 183119 | BAA02g21850 | A02 | 11768607 | C | T | missense_variant | MODERATE | c.3146C>T|p.Ser1049Phe |
S5 |
| 183120 | BAA02g21850 | A02 | 11768950 | G | A | synonymous_variant | LOW | c.3489G>A|p.Arg1163Arg |
S111 |
| 183121 | BAA02g21850 | A02 | 11769111 | C | T | missense_variant | MODERATE | c.3650C>T|p.Thr1217Ile |
S255 |
| 183122 | BAA02g21850 | A02 | 11770762 | G | A | downstream_gene_variant | MODIFIER | c.*515G>A| |
S204 |
| 183123 | BAA02g21850 | A02 | 11770998 | G | A | downstream_gene_variant | MODIFIER | c.*751G>A| |
S295 |
| 183124 | BAA02g21850 | A02 | 11773684 | C | T | downstream_gene_variant | MODIFIER | c.*3437C>T| |
S266 |
| 183125 | BAA02g21870 | A02 | 11774028 | G | A | upstream_gene_variant | MODIFIER | c.-4970G>A| |
S133 |