| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 181551 | BAA02g20930 | A02 | 11159073 | C | T | upstream_gene_variant | MODIFIER | c.-1155G>A| |
S266 |
| 181552 | BAA02g20930 | A02 | 11159369 | G | A | upstream_gene_variant | MODIFIER | c.-1451C>T| |
S37 |
| 181553 | BAA02g20930 | A02 | 11160138 | G | A | upstream_gene_variant | MODIFIER | c.-2220C>T| |
S23 |
| 181554 | BAA02g20930 | A02 | 11160817 | C | T | upstream_gene_variant | MODIFIER | c.-2899G>A| |
S252 |
| 181555 | BAA02g20930 | A02 | 11160938 | G | A | upstream_gene_variant | MODIFIER | c.-3020C>T| |
S240 S281 |
| 181556 | BAA02g20940 | A02 | 11163476 | G | A | synonymous_variant | LOW | c.243C>T|p.Pro81Pro |
S223 |
| 181557 | BAA02g20940 | A02 | 11164576 | C | T | upstream_gene_variant | MODIFIER | c.-566G>A| |
S262 |
| 181558 | BAA02g20940 | A02 | 11164770 | C | T | upstream_gene_variant | MODIFIER | c.-760G>A| |
S289 S290 |
| 181559 | BAA02g20940 | A02 | 11165615 | C | T | upstream_gene_variant | MODIFIER | c.-1605G>A| |
S193 |
| 181560 | BAA02g20940 | A02 | 11166141 | G | A | upstream_gene_variant | MODIFIER | c.-2131C>T| |
S228 |
| 181561 | BAA02g20940 | A02 | 11166966 | A | G | upstream_gene_variant | MODIFIER | c.-2956T>C| |
S274 |
| 181562 | BAA02g20950 | A02 | 11172308 | C | T | missense_variant | MODERATE | c.53G>A|p.Cys18Tyr |
S2 |
| 181563 | BAA02g20950 | A02 | 11172578 | C | T | upstream_gene_variant | MODIFIER | c.-218G>A| |
S250 |
| 181564 | BAA02g20950 | A02 | 11172716 | G | A | upstream_gene_variant | MODIFIER | c.-356C>T| |
S200 |
| 181565 | BAA02g20950 | A02 | 11172742 | G | A | upstream_gene_variant | MODIFIER | c.-382C>T| |
S291 |
| 181566 | BAA02g20950 | A02 | 11172826 | G | A | upstream_gene_variant | MODIFIER | c.-466C>T| |
S150 |
| 181567 | BAA02g20960 | A02 | 11175261 | C | T | missense_variant | MODERATE | c.778G>A|p.Ala260Thr |
S185 |
| 181568 | BAA02g20950 | A02 | 11175428 | C | T | upstream_gene_variant | MODIFIER | c.-3068G>A| |
S178 |
| 181569 | BAA02g20960 | A02 | 11176089 | C | T | missense_variant | MODERATE | c.415G>A|p.Asp139Asn |
S183 S198 |
| 181570 | BAA02g20960 | A02 | 11176140 | C | T | missense_variant | MODERATE | c.364G>A|p.Glu122Lys |
S38 |
| 181571 | BAA02g20950 | A02 | 11176546 | C | T | upstream_gene_variant | MODIFIER | c.-4186G>A| |
S183 S198 |
| 181572 | BAA02g20950 | A02 | 11176834 | G | A | upstream_gene_variant | MODIFIER | c.-4474C>T| |
S156 |
| 181573 | BAA02g20960 | A02 | 11177067 | G | A | synonymous_variant | LOW | c.6C>T|p.Ile2Ile |
S34 |
| 181574 | BAA02g20960 | A02 | 11179219 | G | A | upstream_gene_variant | MODIFIER | c.-2147C>T| |
S64 |
| 181575 | BAA02g20960 | A02 | 11180017 | G | A | upstream_gene_variant | MODIFIER | c.-2945C>T| |
S232 |