| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 178251 | BAA02g19200 | A02 | 9972040 | C | T | upstream_gene_variant | MODIFIER | c.-1892G>A| |
S130 |
| 178252 | BAA02g19200 | A02 | 9972824 | A | G | upstream_gene_variant | MODIFIER | c.-2676T>C| |
S284 |
| 178253 | BAA02g19200 | A02 | 9972977 | C | T | upstream_gene_variant | MODIFIER | c.-2829G>A| |
S308 |
| 178254 | BAA02g19200 | A02 | 9973324 | G | A | upstream_gene_variant | MODIFIER | c.-3176C>T| |
S36 |
| 178255 | BAA02g19210 | A02 | 9974851 | G | A | missense_variant | MODERATE | c.196G>A|p.Ala66Thr |
S84 S93 |
| 178256 | BAA02g19210 | A02 | 9975952 | C | T | missense_variant | MODERATE | c.790C>T|p.Leu264Phe |
S100 |
| 178257 | BAA02g19210 | A02 | 9978105 | G | A | downstream_gene_variant | MODIFIER | c.*1127G>A| |
S126 |
| 178258 | BAA02g19210 | A02 | 9978763 | G | A | downstream_gene_variant | MODIFIER | c.*1785G>A| |
S146 |
| 178259 | BAA02g19210 | A02 | 9979124 | T | G | downstream_gene_variant | MODIFIER | c.*2146T>G| |
S140 |
| 178260 | BAA02g19210 | A02 | 9979711 | G | A | downstream_gene_variant | MODIFIER | c.*2733G>A| |
S279 |
| 178261 | BAA02g19210 | A02 | 9980294 | G | A | downstream_gene_variant | MODIFIER | c.*3316G>A| |
S132 S137 S215 |
| 178262 | BAA02g19210 | A02 | 9980764 | G | A | downstream_gene_variant | MODIFIER | c.*3786G>A| |
S162 |
| 178263 | BAA02g19210 | A02 | 9981752 | C | T | downstream_gene_variant | MODIFIER | c.*4774C>T| |
S163 |
| 178264 | BAA02g19230 | A02 | 9982957 | G | A | upstream_gene_variant | MODIFIER | c.-4423G>A| |
S272 |
| 178265 | BAA02g19230 | A02 | 9983063 | G | A | upstream_gene_variant | MODIFIER | c.-4317G>A| |
S127 |
| 178266 | BAA02g19230 | A02 | 9984105 | G | A | upstream_gene_variant | MODIFIER | c.-3275G>A| |
S280 |
| 178267 | BAA02g19220 | A02 | 9984640 | G | A | upstream_gene_variant | MODIFIER | c.-95C>T| |
S279 |
| 178268 | BAA02g19220 | A02 | 9985816 | C | T | upstream_gene_variant | MODIFIER | c.-1271G>A| |
S124 |
| 178269 | BAA02g19220 | A02 | 9987148 | C | T | upstream_gene_variant | MODIFIER | c.-2603G>A| |
S96 |
| 178270 | BAA02g19220 | A02 | 9987158 | C | T | upstream_gene_variant | MODIFIER | c.-2613G>A| |
S73 S91 |
| 178271 | BAA02g19240 | A02 | 9988034 | G | A | missense_variant | MODERATE | c.622C>T|p.Leu208Phe |
S60 |
| 178272 | BAA02g19220 | A02 | 9988251 | G | A | upstream_gene_variant | MODIFIER | c.-3706C>T| |
S177 |
| 178273 | BAA02g19220 | A02 | 9988863 | C | T | upstream_gene_variant | MODIFIER | c.-4318G>A| |
S78 S83 |
| 178274 | BAA02g19230 | A02 | 9990476 | C | T | downstream_gene_variant | MODIFIER | c.*2896C>T| |
S233 |
| 178275 | BAA02g19260 | A02 | 9991894 | G | A | upstream_gene_variant | MODIFIER | c.-3760G>A| |
S223 |