| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 181151 | BAA02g20740 | A02 | 11019823 | C | T | upstream_gene_variant | MODIFIER | c.-302C>T| |
S226 |
| 181152 | BAA02g20740 | A02 | 11020101 | C | T | upstream_gene_variant | MODIFIER | c.-24C>T| |
S123 |
| 181153 | BAA02g20740 | A02 | 11020430 | C | T | synonymous_variant | LOW | c.306C>T|p.Phe102Phe |
S127 |
| 181154 | BAA02g20740 | A02 | 11021051 | C | T | downstream_gene_variant | MODIFIER | c.*552C>T| |
S71 |
| 181155 | BAA02g20750 | A02 | 11022693 | C | T | upstream_gene_variant | MODIFIER | c.-3442C>T| |
S216 |
| 181156 | BAA02g20750 | A02 | 11022849 | G | A | upstream_gene_variant | MODIFIER | c.-3286G>A| |
S264 |
| 181157 | BAA02g20750 | A02 | 11023030 | C | T | upstream_gene_variant | MODIFIER | c.-3105C>T| |
S249 |
| 181158 | BAA02g20750 | A02 | 11025843 | G | A | upstream_gene_variant | MODIFIER | c.-292G>A| |
S297 |
| 181159 | BAA02g20750 | A02 | 11026552 | G | A | missense_variant | MODERATE | c.418G>A|p.Asp140Asn |
S48 |
| 181160 | BAA02g20750 | A02 | 11026641 | G | A | synonymous_variant | LOW | c.507G>A|p.Lys169Lys |
S19 |
| 181161 | BAA02g20750 | A02 | 11027492 | C | T | downstream_gene_variant | MODIFIER | c.*590C>T| |
S165 |
| 181162 | BAA02g20750 | A02 | 11027981 | C | T | downstream_gene_variant | MODIFIER | c.*1079C>T| |
S123 |
| 181163 | BAA02g20760 | A02 | 11029096 | G | A | upstream_gene_variant | MODIFIER | c.-4190G>A| |
S72 |
| 181164 | BAA02g20760 | A02 | 11029347 | C | T | upstream_gene_variant | MODIFIER | c.-3939C>T| |
S302 |
| 181165 | BAA02g20760 | A02 | 11030503 | C | T | upstream_gene_variant | MODIFIER | c.-2783C>T| |
S157 S166 |
| 181166 | BAA02g20760 | A02 | 11030576 | G | A | upstream_gene_variant | MODIFIER | c.-2710G>A| |
S206 S26 |
| 181167 | BAA02g20760 | A02 | 11030854 | G | A | upstream_gene_variant | MODIFIER | c.-2432G>A| |
S155 S211 |
| 181168 | BAA02g20760 | A02 | 11031432 | C | T | upstream_gene_variant | MODIFIER | c.-1854C>T| |
S71 |
| 181169 | BAA02g20760 | A02 | 11033650 | C | T | missense_variant | MODERATE | c.290C>T|p.Thr97Ile |
S144 |
| 181170 | BAA02g20760 | A02 | 11034127 | G | A | missense_variant | MODERATE | c.767G>A|p.Arg256Lys |
S157 |
| 181171 | BAA02g20760 | A02 | 11035102 | C | T | intron_variant | MODIFIER | c.1367-85C>T| |
S179 |
| 181172 | BAA02g20760 | A02 | 11035139 | G | A | intron_variant | MODIFIER | c.1367-48G>A| |
S241 |
| 181173 | BAA02g20760 | A02 | 11036141 | G | A | downstream_gene_variant | MODIFIER | c.*370G>A| |
S303 |
| 181174 | BAA02g20760 | A02 | 11036304 | G | A | downstream_gene_variant | MODIFIER | c.*533G>A| |
S259 |
| 181175 | BAA02g20770 | A02 | 11038940 | G | A | upstream_gene_variant | MODIFIER | c.-3768G>A| |
S235 |