| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 84651 | BAA01g44830 | A01 | 29865326 | C | T | downstream_gene_variant | MODIFIER | c.*3138G>A| |
S74 |
| 84652 | BAA01g44830 | A01 | 29865457 | G | A | downstream_gene_variant | MODIFIER | c.*3007C>T| |
S296 |
| 84653 | BAA01g44830 | A01 | 29865710 | A | G | downstream_gene_variant | MODIFIER | c.*2754T>C| |
S256 |
| 84654 | BAA01g44830 | A01 | 29866848 | G | A | downstream_gene_variant | MODIFIER | c.*1616C>T| |
S280 |
| 84655 | BAA01g44830 | A01 | 29866851 | C | T | downstream_gene_variant | MODIFIER | c.*1613G>A| |
S41 |
| 84656 | BAA01g44820 | A01 | 29867373 | C | T | missense_variant | MODERATE | c.1900C>T|p.Leu634Phe |
S288 |
| 84657 | BAA01g44820 | A01 | 29868376 | C | T | downstream_gene_variant | MODIFIER | c.*328C>T| |
S94 |
| 84658 | BAA01g44830 | A01 | 29869454 | C | T | missense_variant&splice_region_variant | MODERATE | c.191G>A|p.Cys64Tyr |
S62 |
| 84659 | BAA01g44840 | A01 | 29870268 | C | T | missense_variant | MODERATE | c.767G>A|p.Ser256Asn |
S17 |
| 84660 | BAA01g44840 | A01 | 29870326 | C | T | missense_variant | MODERATE | c.709G>A|p.Gly237Arg |
S255 |
| 84661 | BAA01g44840 | A01 | 29871610 | T | G | missense_variant | MODERATE | c.52A>C|p.Lys18Gln |
S159 |
| 84662 | BAA01g44830 | A01 | 29871713 | G | A | upstream_gene_variant | MODIFIER | c.-2069C>T| |
S149 |
| 84663 | BAA01g44830 | A01 | 29872296 | C | T | upstream_gene_variant | MODIFIER | c.-2652G>A| |
S78 S83 |
| 84664 | BAA01g44830 | A01 | 29872530 | C | T | upstream_gene_variant | MODIFIER | c.-2886G>A| |
S210 S225 |
| 84665 | BAA01g44830 | A01 | 29872639 | C | T | upstream_gene_variant | MODIFIER | c.-2995G>A| |
S112 |
| 84666 | BAA01g44830 | A01 | 29873201 | C | T | upstream_gene_variant | MODIFIER | c.-3557G>A| |
S244 |
| 84667 | BAA01g44830 | A01 | 29873204 | A | T | upstream_gene_variant | MODIFIER | c.-3560T>A| |
S244 |
| 84668 | BAA01g44850 | A01 | 29874102 | C | T | missense_variant | MODERATE | c.55C>T|p.Pro19Ser |
S74 |
| 84669 | BAA01g44850 | A01 | 29874261 | G | A | synonymous_variant | LOW | c.129G>A|p.Lys43Lys |
S175 |
| 84670 | BAA01g44850 | A01 | 29874630 | G | A | synonymous_variant | LOW | c.399G>A|p.Gln133Gln |
S104 |
| 84671 | BAA01g44850 | A01 | 29874775 | C | T | missense_variant | MODERATE | c.463C>T|p.Pro155Ser |
S153 S213 |
| 84672 | BAA01g44840 | A01 | 29875177 | G | A | upstream_gene_variant | MODIFIER | c.-3516C>T| |
S199 |
| 84673 | BAA01g44860 | A01 | 29876161 | C | T | missense_variant | MODERATE | c.1051G>A|p.Val351Ile |
S200 |
| 84674 | BAA01g44840 | A01 | 29876330 | C | T | upstream_gene_variant | MODIFIER | c.-4669G>A| |
S62 |
| 84675 | BAA01g44840 | A01 | 29876435 | G | A | upstream_gene_variant | MODIFIER | c.-4774C>T| |
S298 |