| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 88251 | BAA01g47060 | A01 | 31339114 | C | T | upstream_gene_variant | MODIFIER | c.-3469G>A| |
S115 |
| 88252 | BAA01g47060 | A01 | 31339223 | C | T | upstream_gene_variant | MODIFIER | c.-3578G>A| |
S110 |
| 88253 | BAA01g47060 | A01 | 31339728 | C | T | upstream_gene_variant | MODIFIER | c.-4083G>A| |
S202 |
| 88254 | BAA01g47060 | A01 | 31339756 | C | T | upstream_gene_variant | MODIFIER | c.-4111G>A| |
S144 |
| 88255 | BAA01g47060 | A01 | 31340158 | C | T | upstream_gene_variant | MODIFIER | c.-4513G>A| |
S95 |
| 88256 | BAA01g47060-BAA01g47070 | A01 | 31341268 | C | T | intergenic_region | MODIFIER | n.31341268C>T| |
S100 |
| 88257 | BAA01g47070 | A01 | 31342473 | C | T | downstream_gene_variant | MODIFIER | c.*4338G>A| |
S302 |
| 88258 | BAA01g47070 | A01 | 31342575 | G | A | downstream_gene_variant | MODIFIER | c.*4236C>T| |
S127 |
| 88259 | BAA01g47070 | A01 | 31344321 | C | T | downstream_gene_variant | MODIFIER | c.*2490G>A| |
S142 |
| 88260 | BAA01g47080 | A01 | 31347398 | G | A | downstream_gene_variant | MODIFIER | c.*2031C>T| |
S79 S84 |
| 88261 | BAA01g47080 | A01 | 31347768 | C | T | downstream_gene_variant | MODIFIER | c.*1661G>A| |
S172 S217 |
| 88262 | BAA01g47080 | A01 | 31347819 | C | T | downstream_gene_variant | MODIFIER | c.*1610G>A| |
S297 |
| 88263 | BAA01g47070 | A01 | 31348109 | C | T | synonymous_variant | LOW | c.267G>A|p.Gly89Gly |
S71 |
| 88264 | BAA01g47080 | A01 | 31350040 | C | T | missense_variant | MODERATE | c.898G>A|p.Glu300Lys |
S287 |
| 88265 | BAA01g47070 | A01 | 31351178 | G | A | upstream_gene_variant | MODIFIER | c.-2538C>T| |
S277 |
| 88266 | BAA01g47090 | A01 | 31352218 | G | A | synonymous_variant | LOW | c.2082C>T|p.Ile694Ile |
S221 |
| 88267 | BAA01g47070 | A01 | 31352427 | C | T | upstream_gene_variant | MODIFIER | c.-3787G>A| |
S308 |
| 88268 | BAA01g47090 | A01 | 31353883 | G | A | synonymous_variant | LOW | c.1275C>T|p.Leu425Leu |
S16 |
| 88269 | BAA01g47090 | A01 | 31354156 | C | T | synonymous_variant | LOW | c.1092G>A|p.Glu364Glu |
S219 S72 |
| 88270 | BAA01g47090 | A01 | 31354735 | C | T | synonymous_variant | LOW | c.672G>A|p.Lys224Lys |
S199 |
| 88271 | BAA01g47090 | A01 | 31355002 | C | T | missense_variant | MODERATE | c.490G>A|p.Asp164Asn |
S155 S187 |
| 88272 | BAA01g47090 | A01 | 31355294 | C | T | stop_gained | HIGH | c.198G>A|p.Trp66* |
S114 |
| 88273 | BAA01g47100 | A01 | 31356196 | C | T | missense_variant | MODERATE | c.1997G>A|p.Arg666Lys |
S181 |
| 88274 | BAA01g47100 | A01 | 31356224 | C | T | missense_variant | MODERATE | c.1969G>A|p.Glu657Lys |
S155 |
| 88275 | BAA01g47100 | A01 | 31357836 | G | A | synonymous_variant | LOW | c.777C>T|p.Phe259Phe |
S44 |