| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 71451 | BAA01g37390 | A01 | 24976049 | C | T | downstream_gene_variant | MODIFIER | c.*3050C>T| |
S170 |
| 71452 | BAA01g37420 | A01 | 24982388 | C | T | upstream_gene_variant | MODIFIER | c.-4716C>T| |
S112 |
| 71453 | BAA01g37410 | A01 | 24983028 | G | A | missense_variant | MODERATE | c.266C>T|p.Ala89Val |
S15 S3 |
| 71454 | BAA01g37420 | A01 | 24983176 | G | A | upstream_gene_variant | MODIFIER | c.-3928G>A| |
S110 |
| 71455 | BAA01g37410 | A01 | 24984569 | C | T | upstream_gene_variant | MODIFIER | c.-1101G>A| |
S42 |
| 71456 | BAA01g37410 | A01 | 24985506 | G | A | upstream_gene_variant | MODIFIER | c.-2038C>T| |
S172 |
| 71457 | BAA01g37410 | A01 | 24985901 | C | T | upstream_gene_variant | MODIFIER | c.-2433G>A| |
S249 |
| 71458 | BAA01g37420 | A01 | 24987190 | C | T | synonymous_variant | LOW | c.87C>T|p.Asp29Asp |
S78 S83 |
| 71459 | BAA01g37430 | A01 | 24988852 | G | A | missense_variant | MODERATE | c.214G>A|p.Gly72Arg |
S271 |
| 71460 | BAA01g37430 | A01 | 24989043 | G | A | synonymous_variant | LOW | c.405G>A|p.Gln135Gln |
S217 S248 |
| 71461 | BAA01g37420 | A01 | 24989474 | C | T | downstream_gene_variant | MODIFIER | c.*1723C>T| |
S12 |
| 71462 | BAA01g37420 | A01 | 24989651 | C | T | downstream_gene_variant | MODIFIER | c.*1900C>T| |
S233 |
| 71463 | BAA01g37420 | A01 | 24990510 | C | T | downstream_gene_variant | MODIFIER | c.*2759C>T| |
S128 |
| 71464 | BAA01g37440 | A01 | 24991475 | C | T | upstream_gene_variant | MODIFIER | c.-14G>A| |
S233 |
| 71465 | BAA01g37440 | A01 | 24993679 | G | A | upstream_gene_variant | MODIFIER | c.-2218C>T| |
S143 |
| 71466 | BAA01g37440 | A01 | 24993915 | A | T | upstream_gene_variant | MODIFIER | c.-2454T>A| |
S116 |
| 71467 | BAA01g37440 | A01 | 24993918 | C | G | upstream_gene_variant | MODIFIER | c.-2457G>C| |
S116 |
| 71468 | BAA01g37440 | A01 | 24994913 | G | A | upstream_gene_variant | MODIFIER | c.-3452C>T| |
S294 |
| 71469 | BAA01g37440 | A01 | 24995404 | C | T | upstream_gene_variant | MODIFIER | c.-3943G>A| |
S150 |
| 71470 | BAA01g37440 | A01 | 24995803 | C | T | upstream_gene_variant | MODIFIER | c.-4342G>A| |
S270 |
| 71471 | BAA01g37440 | A01 | 24995980 | C | T | upstream_gene_variant | MODIFIER | c.-4519G>A| |
S11 |
| 71472 | BAA01g37470 | A01 | 25001024 | G | A | upstream_gene_variant | MODIFIER | c.-4271G>A| |
S86 |
| 71473 | BAA01g37470 | A01 | 25001452 | C | T | upstream_gene_variant | MODIFIER | c.-3843C>T| |
S74 |
| 71474 | BAA01g37470 | A01 | 25001567 | C | T | upstream_gene_variant | MODIFIER | c.-3728C>T| |
S104 S52 |
| 71475 | BAA01g37460 | A01 | 25002056 | C | T | upstream_gene_variant | MODIFIER | c.-46G>A| |
S211 |