| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 190851 | BAA02g26090 | A02 | 14466689 | G | A | upstream_gene_variant | MODIFIER | c.-2920C>T| |
S129 |
| 190852 | BAA02g26090 | A02 | 14466829 | C | T | upstream_gene_variant | MODIFIER | c.-3060G>A| |
S79 S84 |
| 190853 | BAA02g26090 | A02 | 14466910 | C | T | upstream_gene_variant | MODIFIER | c.-3141G>A| |
S167 |
| 190854 | BAA02g26090 | A02 | 14466919 | A | T | upstream_gene_variant | MODIFIER | c.-3150T>A| |
S271 |
| 190855 | BAA02g26090 | A02 | 14466955 | G | A | upstream_gene_variant | MODIFIER | c.-3186C>T| |
S72 S78 |
| 190856 | BAA02g26090 | A02 | 14468242 | G | A | upstream_gene_variant | MODIFIER | c.-4473C>T| |
S128 |
| 190857 | BAA02g26100 | A02 | 14468991 | C | T | upstream_gene_variant | MODIFIER | c.-2356G>A| |
S183 S198 |
| 190858 | BAA02g26100 | A02 | 14469103 | C | T | upstream_gene_variant | MODIFIER | c.-2468G>A| |
S250 |
| 190859 | BAA02g26100 | A02 | 14469737 | G | A | upstream_gene_variant | MODIFIER | c.-3102C>T| |
S228 |
| 190860 | BAA02g26100 | A02 | 14471536 | C | T | upstream_gene_variant | MODIFIER | c.-4901G>A| |
S54 |
| 190861 | BAA02g26100 | A02 | 14471624 | C | T | upstream_gene_variant | MODIFIER | c.-4989G>A| |
S180 |
| 190862 | BAA02g26120 | A02 | 14472442 | C | T | missense_variant | MODERATE | c.124G>A|p.Glu42Lys |
S192 |
| 190863 | BAA02g26120 | A02 | 14472534 | C | T | missense_variant | MODERATE | c.32G>A|p.Arg11Gln |
S305 |
| 190864 | BAA02g26120 | A02 | 14472613 | C | T | upstream_gene_variant | MODIFIER | c.-48G>A| |
S224 |
| 190865 | BAA02g26120 | A02 | 14473476 | C | T | upstream_gene_variant | MODIFIER | c.-911G>A| |
S53 |
| 190866 | BAA02g26130 | A02 | 14473866 | C | T | synonymous_variant | LOW | c.183C>T|p.Asp61Asp |
S32 |
| 190867 | BAA02g26130 | A02 | 14474187 | G | A | synonymous_variant | LOW | c.504G>A|p.Ala168Ala |
S80 |
| 190868 | BAA02g26130 | A02 | 14474247 | C | T | synonymous_variant | LOW | c.564C>T|p.Phe188Phe |
S2 |
| 190869 | BAA02g26130 | A02 | 14475114 | G | A | missense_variant | MODERATE | c.730G>A|p.Asp244Asn |
S80 |
| 190870 | BAA02g26120 | A02 | 14476149 | G | A | upstream_gene_variant | MODIFIER | c.-3584C>T| |
S153 S213 |
| 190871 | BAA02g26130 | A02 | 14478581 | C | T | downstream_gene_variant | MODIFIER | c.*2779C>T| |
S16 |
| 190872 | BAA02g26140 | A02 | 14480858 | C | T | synonymous_variant | LOW | c.1125G>A|p.Gln375Gln |
S178 |
| 190873 | BAA02g26140 | A02 | 14481708 | G | C | stop_gained | HIGH | c.576C>G|p.Tyr192* |
S196 |
| 190874 | BAA02g26140 | A02 | 14481840 | C | T | stop_gained | HIGH | c.444G>A|p.Trp148* |
S224 |
| 190875 | BAA02g26140 | A02 | 14482035 | G | A | synonymous_variant | LOW | c.249C>T|p.Leu83Leu |
S256 |