| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 31451 | BAA01g21810 | A01 | 10868900 | G | A | upstream_gene_variant | MODIFIER | c.-458G>A| |
S149 |
| 31452 | BAA01g21810 | A01 | 10869191 | C | T | upstream_gene_variant | MODIFIER | c.-167C>T| |
S36 |
| 31453 | BAA01g21810 | A01 | 10869311 | G | A | upstream_gene_variant | MODIFIER | c.-47G>A| |
S165 |
| 31454 | BAA01g21810 | A01 | 10869635 | G | A | missense_variant | MODERATE | c.278G>A|p.Gly93Glu |
S268 |
| 31455 | BAA01g21820 | A01 | 10870358 | G | A | upstream_gene_variant | MODIFIER | c.-156C>T| |
S181 |
| 31456 | BAA01g21820 | A01 | 10870759 | C | T | upstream_gene_variant | MODIFIER | c.-557G>A| |
S159 S243 S276 S298 S299 |
| 31457 | BAA01g21820 | A01 | 10870775 | C | T | upstream_gene_variant | MODIFIER | c.-573G>A| |
S168 |
| 31458 | BAA01g21820 | A01 | 10870782 | C | T | upstream_gene_variant | MODIFIER | c.-580G>A| |
S135 |
| 31459 | BAA01g21820 | A01 | 10871589 | G | A | upstream_gene_variant | MODIFIER | c.-1387C>T| |
S33 |
| 31460 | BAA01g21820 | A01 | 10871631 | C | T | upstream_gene_variant | MODIFIER | c.-1429G>A| |
S88 |
| 31461 | BAA01g21840 | A01 | 10872507 | G | A | synonymous_variant | LOW | c.222C>T|p.Arg74Arg |
S111 |
| 31462 | BAA01g21820 | A01 | 10873164 | G | A | upstream_gene_variant | MODIFIER | c.-2962C>T| |
S302 |
| 31463 | BAA01g21820 | A01 | 10873204 | C | T | upstream_gene_variant | MODIFIER | c.-3002G>A| |
S167 |
| 31464 | BAA01g21820 | A01 | 10873608 | G | A | upstream_gene_variant | MODIFIER | c.-3406C>T| |
S193 |
| 31465 | BAA01g21820 | A01 | 10874289 | C | T | upstream_gene_variant | MODIFIER | c.-4087G>A| |
S183 |
| 31466 | BAA01g21820 | A01 | 10874573 | G | A | upstream_gene_variant | MODIFIER | c.-4371C>T| |
S84 S93 |
| 31467 | BAA01g21830 | A01 | 10875610 | G | A | upstream_gene_variant | MODIFIER | c.-4228C>T| |
S139 S215 |
| 31468 | BAA01g21830 | A01 | 10875792 | A | T | upstream_gene_variant | MODIFIER | c.-4410T>A| |
S187 |
| 31469 | BAA01g21860 | A01 | 10876980 | G | A | missense_variant | MODERATE | c.2005C>T|p.Pro669Ser |
S251 S297 |
| 31470 | BAA01g21860 | A01 | 10877094 | G | A | missense_variant | MODERATE | c.1891C>T|p.Pro631Ser |
S27 |
| 31471 | BAA01g21860 | A01 | 10877098 | C | T | synonymous_variant | LOW | c.1887G>A|p.Glu629Glu |
S158 |
| 31472 | BAA01g21860 | A01 | 10878228 | C | T | missense_variant | MODERATE | c.757G>A|p.Ala253Thr |
S158 |
| 31473 | BAA01g21860 | A01 | 10878898 | G | A | synonymous_variant | LOW | c.87C>T|p.Thr29Thr |
S174 |
| 31474 | BAA01g21850 | A01 | 10879056 | G | A | upstream_gene_variant | MODIFIER | c.-2601C>T| |
S263 |
| 31475 | BAA01g21850 | A01 | 10880312 | C | T | upstream_gene_variant | MODIFIER | c.-3857G>A| |
S136 |