| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 115301 | BAA10g09730 | A10 | 11622457 | C | T | upstream_gene_variant | MODIFIER | c.-924C>T| |
S164 |
| 115302 | BAA10g09730 | A10 | 11623089 | G | A | upstream_gene_variant | MODIFIER | c.-292G>A| |
S189 |
| 115303 | BAA10g09730 | A10 | 11626482 | G | A | downstream_gene_variant | MODIFIER | c.*2526G>A| |
S231 |
| 115304 | BAA10g09730 | A10 | 11626626 | G | A | downstream_gene_variant | MODIFIER | c.*2670G>A| |
S264 |
| 115305 | BAA10g09730 | A10 | 11627261 | C | T | downstream_gene_variant | MODIFIER | c.*3305C>T| |
S265 |
| 115306 | BAA10g09730 | A10 | 11627263 | C | T | downstream_gene_variant | MODIFIER | c.*3307C>T| |
S224 |
| 115307 | BAA10g09740 | A10 | 11628947 | C | T | upstream_gene_variant | MODIFIER | c.-1089G>A| |
S275 |
| 115308 | BAA10g09740 | A10 | 11629056 | G | A | upstream_gene_variant | MODIFIER | c.-1198C>T| |
S252 |
| 115309 | BAA10g09740 | A10 | 11629110 | C | T | upstream_gene_variant | MODIFIER | c.-1252G>A| |
S282 |
| 115310 | BAA10g09740 | A10 | 11629142 | C | T | upstream_gene_variant | MODIFIER | c.-1284G>A| |
S44 |
| 115311 | BAA10g09740 | A10 | 11629379 | T | G | upstream_gene_variant | MODIFIER | c.-1521A>C| |
S245 |
| 115312 | BAA10g09740 | A10 | 11629567 | C | T | upstream_gene_variant | MODIFIER | c.-1709G>A| |
S170 |
| 115313 | BAA10g09740 | A10 | 11630000 | G | A | upstream_gene_variant | MODIFIER | c.-2142C>T| |
S68 |
| 115314 | BAA10g09740 | A10 | 11630716 | C | T | upstream_gene_variant | MODIFIER | c.-2858G>A| |
S225 S73 |
| 115315 | BAA10g09750 | A10 | 11633265 | C | T | downstream_gene_variant | MODIFIER | c.*2058G>A| |
S266 |
| 115316 | BAA10g09750 | A10 | 11636067 | C | T | missense_variant | MODERATE | c.394G>A|p.Val132Ile |
S162 |
| 115317 | BAA10g09760 | A10 | 11636432 | G | A | upstream_gene_variant | MODIFIER | c.-4667G>A| |
S80 |
| 115318 | BAA10g09760 | A10 | 11636811 | C | T | upstream_gene_variant | MODIFIER | c.-4288C>T| |
S38 |
| 115319 | BAA10g09760 | A10 | 11637378 | G | A | upstream_gene_variant | MODIFIER | c.-3721G>A| |
S120 |
| 115320 | BAA10g09750 | A10 | 11637692 | C | T | synonymous_variant | LOW | c.174G>A|p.Glu58Glu |
S235 |
| 115321 | BAA10g09750 | A10 | 11637991 | G | A | synonymous_variant | LOW | c.84C>T|p.Phe28Phe |
S290 |
| 115322 | BAA10g09750 | A10 | 11638466 | C | T | upstream_gene_variant | MODIFIER | c.-392G>A| |
S256 |
| 115323 | BAA10g09750 | A10 | 11639228 | G | A | upstream_gene_variant | MODIFIER | c.-1154C>T| |
S59 |
| 115324 | BAA10g09750 | A10 | 11640144 | G | A | upstream_gene_variant | MODIFIER | c.-2070C>T| |
S228 |
| 115325 | BAA10g09750 | A10 | 11640780 | G | A | upstream_gene_variant | MODIFIER | c.-2706C>T| |
S192 |