| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 179651 | BAA02g19950 | A02 | 10473590 | G | A | missense_variant | MODERATE | c.403G>A|p.Asp135Asn |
S303 |
| 179652 | BAA02g19950 | A02 | 10473850 | G | A | synonymous_variant | LOW | c.663G>A|p.Glu221Glu |
S190 |
| 179653 | BAA02g19950 | A02 | 10475340 | G | A | missense_variant | MODERATE | c.2153G>A|p.Gly718Glu |
S286 |
| 179654 | BAA02g19950 | A02 | 10475703 | C | T | missense_variant | MODERATE | c.2516C>T|p.Ser839Phe |
S40 S49 |
| 179655 | BAA02g19950 | A02 | 10475845 | G | A | synonymous_variant | LOW | c.2658G>A|p.Arg886Arg |
S247 |
| 179656 | BAA02g19960 | A02 | 10476814 | G | A | downstream_gene_variant | MODIFIER | c.*1175C>T| |
S62 |
| 179657 | BAA02g19950 | A02 | 10477458 | G | A | downstream_gene_variant | MODIFIER | c.*56G>A| |
S206 S26 |
| 179658 | BAA02g19960 | A02 | 10478012 | C | T | missense_variant | MODERATE | c.460G>A|p.Asp154Asn |
S196 |
| 179659 | BAA02g19960 | A02 | 10478740 | G | A | synonymous_variant | LOW | c.36C>T|p.Ile12Ile |
S132 S137 |
| 179660 | BAA02g19960 | A02 | 10479544 | G | A | upstream_gene_variant | MODIFIER | c.-769C>T| |
S139 |
| 179661 | BAA02g19970 | A02 | 10482092 | G | A | missense_variant | MODERATE | c.1816C>T|p.Leu606Phe |
S136 |
| 179662 | BAA02g19970 | A02 | 10484088 | C | T | missense_variant | MODERATE | c.574G>A|p.Glu192Lys |
S244 |
| 179663 | BAA02g19970 | A02 | 10485362 | C | T | upstream_gene_variant | MODIFIER | c.-515G>A| |
S195 |
| 179664 | BAA02g19970 | A02 | 10485424 | G | A | upstream_gene_variant | MODIFIER | c.-577C>T| |
S278 |
| 179665 | BAA02g19970 | A02 | 10485518 | C | T | upstream_gene_variant | MODIFIER | c.-671G>A| |
S182 |
| 179666 | BAA02g19970 | A02 | 10485533 | G | A | upstream_gene_variant | MODIFIER | c.-686C>T| |
S148 S30 S31 |
| 179667 | BAA02g19970 | A02 | 10486945 | C | T | upstream_gene_variant | MODIFIER | c.-2098G>A| |
S80 |
| 179668 | BAA02g19970 | A02 | 10487283 | C | T | upstream_gene_variant | MODIFIER | c.-2436G>A| |
S293 |
| 179669 | BAA02g19970 | A02 | 10489002 | G | A | upstream_gene_variant | MODIFIER | c.-4155C>T| |
S190 |
| 179670 | BAA02g19970 | A02 | 10489809 | C | T | upstream_gene_variant | MODIFIER | c.-4962G>A| |
S180 |
| 179671 | BAA02g19970-BAA02g19980 | A02 | 10490090 | C | T | intergenic_region | MODIFIER | n.10490090C>T| |
S75 S81 |
| 179672 | BAA02g19970-BAA02g19980 | A02 | 10490574 | G | A | intergenic_region | MODIFIER | n.10490574G>A| |
S125 |
| 179673 | BAA02g19970-BAA02g19980 | A02 | 10492853 | G | A | intergenic_region | MODIFIER | n.10492853G>A| |
S232 |
| 179674 | BAA02g19970-BAA02g19980 | A02 | 10493126 | G | A | intergenic_region | MODIFIER | n.10493126G>A| |
S143 |
| 179675 | BAA02g19970-BAA02g19980 | A02 | 10493185 | G | A | intergenic_region | MODIFIER | n.10493185G>A| |
S272 |