| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 26201 | BAA01g18680 | A01 | 9175165 | C | T | upstream_gene_variant | MODIFIER | c.-2161G>A| |
S62 |
| 26202 | BAA01g18680 | A01 | 9176131 | G | A | upstream_gene_variant | MODIFIER | c.-3127C>T| |
S144 |
| 26203 | BAA01g18680 | A01 | 9177544 | C | T | upstream_gene_variant | MODIFIER | c.-4540G>A| |
S205 |
| 26204 | BAA01g18680-BAA01g18690 | A01 | 9178081 | C | T | intergenic_region | MODIFIER | n.9178081C>T| |
S42 |
| 26205 | BAA01g18690 | A01 | 9182942 | C | T | upstream_gene_variant | MODIFIER | c.-2101C>T| |
S192 |
| 26206 | BAA01g18690 | A01 | 9184519 | G | A | upstream_gene_variant | MODIFIER | c.-524G>A| |
S292 |
| 26207 | BAA01g18690 | A01 | 9185326 | G | A | missense_variant | MODERATE | c.208G>A|p.Glu70Lys |
S208 S219 |
| 26208 | BAA01g18690 | A01 | 9186399 | C | T | intron_variant | MODIFIER | c.888+9C>T| |
S272 |
| 26209 | BAA01g18690 | A01 | 9186438 | C | T | intron_variant | MODIFIER | c.888+48C>T| |
S120 |
| 26210 | BAA01g18690 | A01 | 9186896 | C | T | intron_variant | MODIFIER | c.1100+10C>T| |
S128 |
| 26211 | BAA01g18690 | A01 | 9187965 | G | A | intron_variant | MODIFIER | c.1709-26G>A| |
S251 |
| 26212 | BAA01g18700 | A01 | 9188625 | G | A | upstream_gene_variant | MODIFIER | c.-4739G>A| |
S244 |
| 26213 | BAA01g18700 | A01 | 9189396 | C | T | upstream_gene_variant | MODIFIER | c.-3968C>T| |
S7 |
| 26214 | BAA01g18700 | A01 | 9189428 | C | T | upstream_gene_variant | MODIFIER | c.-3936C>T| |
S228 |
| 26215 | BAA01g18700 | A01 | 9192803 | C | T | upstream_gene_variant | MODIFIER | c.-561C>T| |
S146 |
| 26216 | BAA01g18700 | A01 | 9193112 | C | T | upstream_gene_variant | MODIFIER | c.-252C>T| |
S134 |
| 26217 | BAA01g18700 | A01 | 9193601 | C | T | missense_variant | MODERATE | c.238C>T|p.Pro80Ser |
S206 S26 |
| 26218 | BAA01g18700 | A01 | 9193863 | C | T | missense_variant | MODERATE | c.500C>T|p.Thr167Ile |
S277 |
| 26219 | BAA01g18700 | A01 | 9194330 | G | A | splice_region_variant&intron_variant | LOW | c.868-4G>A| |
S86 |
| 26220 | BAA01g18700 | A01 | 9195288 | C | T | intron_variant | MODIFIER | c.1432-20C>T| |
S128 |
| 26221 | BAA01g18700 | A01 | 9195650 | C | T | intron_variant | MODIFIER | c.1638+30C>T| |
S267 |
| 26222 | BAA01g18700 | A01 | 9195814 | G | A | intron_variant | MODIFIER | c.1729+15G>A| |
S116 |
| 26223 | BAA01g18700 | A01 | 9195915 | G | A | missense_variant | MODERATE | c.1744G>A|p.Asp582Asn |
S240 |
| 26224 | BAA01g18700 | A01 | 9198119 | G | A | downstream_gene_variant | MODIFIER | c.*1070G>A| |
S123 |
| 26225 | BAA01g18700 | A01 | 9198189 | G | A | downstream_gene_variant | MODIFIER | c.*1140G>A| |
S159 S243 |