| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 43601 | BAA01g26690 | A01 | 14977822 | C | T | missense_variant | MODERATE | c.283G>A|p.Asp95Asn |
S211 S227 |
| 43602 | BAA01g26690 | A01 | 14978073 | C | T | missense_variant | MODERATE | c.32G>A|p.Gly11Glu |
S67 |
| 43603 | BAA01g26690 | A01 | 14978111 | C | T | upstream_gene_variant | MODIFIER | c.-7G>A| |
S125 |
| 43604 | BAA01g26690 | A01 | 14978155 | G | A | upstream_gene_variant | MODIFIER | c.-51C>T| |
S33 |
| 43605 | BAA01g26690 | A01 | 14979897 | G | A | upstream_gene_variant | MODIFIER | c.-1793C>T| |
S109 |
| 43606 | BAA01g26690 | A01 | 14982821 | C | T | upstream_gene_variant | MODIFIER | c.-4717G>A| |
S255 |
| 43607 | BAA01g26690 | A01 | 14983057 | G | A | upstream_gene_variant | MODIFIER | c.-4953C>T| |
S236 |
| 43608 | BAA01g26690-BAA01g26700 | A01 | 14984273 | C | T | intergenic_region | MODIFIER | n.14984273C>T| |
S255 |
| 43609 | BAA01g26690-BAA01g26700 | A01 | 14984443 | G | A | intergenic_region | MODIFIER | n.14984443G>A| |
S287 |
| 43610 | BAA01g26700 | A01 | 14985457 | G | A | upstream_gene_variant | MODIFIER | c.-4648G>A| |
S163 |
| 43611 | BAA01g26700 | A01 | 14985659 | G | A | upstream_gene_variant | MODIFIER | c.-4446G>A| |
S57 |
| 43612 | BAA01g26700 | A01 | 14986018 | G | A | upstream_gene_variant | MODIFIER | c.-4087G>A| |
S110 |
| 43613 | BAA01g26700 | A01 | 14986636 | C | T | upstream_gene_variant | MODIFIER | c.-3469C>T| |
S135 |
| 43614 | BAA01g26700 | A01 | 14987546 | G | A | upstream_gene_variant | MODIFIER | c.-2559G>A| |
S169 |
| 43615 | BAA01g26700 | A01 | 14988227 | G | A | upstream_gene_variant | MODIFIER | c.-1878G>A| |
S294 |
| 43616 | BAA01g26700 | A01 | 14989120 | G | A | upstream_gene_variant | MODIFIER | c.-985G>A| |
S278 |
| 43617 | BAA01g26700 | A01 | 14989221 | G | A | upstream_gene_variant | MODIFIER | c.-884G>A| |
S13 S140 S168 S219 S279 |
| 43618 | BAA01g26700 | A01 | 14989354 | A | G | upstream_gene_variant | MODIFIER | c.-751A>G| |
S13 |
| 43619 | BAA01g26700 | A01 | 14989423 | C | T | upstream_gene_variant | MODIFIER | c.-682C>T| |
S270 |
| 43620 | BAA01g26700 | A01 | 14989471 | C | T | upstream_gene_variant | MODIFIER | c.-634C>T| |
S117 |
| 43621 | BAA01g26710 | A01 | 14990873 | C | T | upstream_gene_variant | MODIFIER | c.-824C>T| |
S134 |
| 43622 | BAA01g26710 | A01 | 14992438 | C | T | missense_variant | MODERATE | c.103C>T|p.Arg35Cys |
S142 |
| 43623 | BAA01g26700 | A01 | 14993001 | G | A | downstream_gene_variant | MODIFIER | c.*2331G>A| |
S23 |
| 43624 | BAA01g26700 | A01 | 14993360 | C | T | downstream_gene_variant | MODIFIER | c.*2690C>T| |
S46 |
| 43625 | BAA01g26710 | A01 | 14994357 | C | T | missense_variant | MODERATE | c.805C>T|p.Pro269Ser |
S282 |