| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 106351 | BAA10g08250-BAA10g08260 | A10 | 6023268 | G | A | intergenic_region | MODIFIER | n.6023268G>A| |
S55 |
| 106352 | BAA10g08250-BAA10g08260 | A10 | 6023405 | C | T | intergenic_region | MODIFIER | n.6023405C>T| |
S51 |
| 106353 | BAA10g08250-BAA10g08260 | A10 | 6023889 | T | C | intergenic_region | MODIFIER | n.6023889T>C| |
S82 S83 S92 |
| 106354 | BAA10g08250-BAA10g08260 | A10 | 6024857 | C | T | intergenic_region | MODIFIER | n.6024857C>T| |
S183 |
| 106355 | BAA10g08250-BAA10g08260 | A10 | 6025097 | C | T | intergenic_region | MODIFIER | n.6025097C>T| |
S11 |
| 106356 | BAA10g08250-BAA10g08260 | A10 | 6025137 | G | A | intergenic_region | MODIFIER | n.6025137G>A| |
S118 |
| 106357 | BAA10g08260 | A10 | 6026206 | G | A | upstream_gene_variant | MODIFIER | c.-4019G>A| |
S295 |
| 106358 | BAA10g08260 | A10 | 6026229 | C | T | upstream_gene_variant | MODIFIER | c.-3996C>T| |
S166 |
| 106359 | BAA10g08260 | A10 | 6026408 | C | T | upstream_gene_variant | MODIFIER | c.-3817C>T| |
S266 |
| 106360 | BAA10g08260 | A10 | 6026480 | G | A | upstream_gene_variant | MODIFIER | c.-3745G>A| |
S69 |
| 106361 | BAA10g08260 | A10 | 6026682 | G | A | upstream_gene_variant | MODIFIER | c.-3543G>A| |
S226 |
| 106362 | BAA10g08260 | A10 | 6026761 | G | A | upstream_gene_variant | MODIFIER | c.-3464G>A| |
S290 |
| 106363 | BAA10g08260 | A10 | 6026885 | A | C | upstream_gene_variant | MODIFIER | c.-3340A>C| |
S2 |
| 106364 | BAA10g08260 | A10 | 6027771 | G | A | upstream_gene_variant | MODIFIER | c.-2454G>A| |
S92 |
| 106365 | BAA10g08260 | A10 | 6028695 | G | A | upstream_gene_variant | MODIFIER | c.-1530G>A| |
S306 S308 |
| 106366 | BAA10g08260 | A10 | 6029307 | C | T | upstream_gene_variant | MODIFIER | c.-918C>T| |
S263 |
| 106367 | BAA10g08260 | A10 | 6030603 | G | A | missense_variant | MODERATE | c.379G>A|p.Glu127Lys |
S120 |
| 106368 | BAA10g08260 | A10 | 6031131 | G | A | missense_variant | MODERATE | c.811G>A|p.Val271Ile |
S140 |
| 106369 | BAA10g08260 | A10 | 6031696 | C | T | missense_variant | MODERATE | c.1139C>T|p.Ser380Leu |
S286 |
| 106370 | BAA10g08260 | A10 | 6032180 | C | T | synonymous_variant | LOW | c.1467C>T|p.Arg489Arg |
S237 |
| 106371 | BAA10g08260 | A10 | 6032362 | G | A | stop_gained | HIGH | c.1572G>A|p.Trp524* |
S184 |
| 106372 | BAA10g08260 | A10 | 6032460 | A | G | intron_variant | MODIFIER | c.1602+68A>G| |
S32 |
| 106373 | BAA10g08260 | A10 | 6033977 | G | A | downstream_gene_variant | MODIFIER | c.*734G>A| |
S296 |
| 106374 | BAA10g08260 | A10 | 6034140 | G | A | downstream_gene_variant | MODIFIER | c.*897G>A| |
S83 |
| 106375 | BAA10g08260 | A10 | 6034472 | G | A | downstream_gene_variant | MODIFIER | c.*1229G>A| |
S293 |