| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 17601 | BAA01g13250 | A01 | 6293369 | C | T | upstream_gene_variant | MODIFIER | c.-4936G>A| |
S10 |
| 17602 | BAA01g13260 | A01 | 6294134 | G | A | upstream_gene_variant | MODIFIER | c.-4052C>T| |
S240 |
| 17603 | BAA01g13260 | A01 | 6294475 | C | T | upstream_gene_variant | MODIFIER | c.-4393G>A| |
S19 |
| 17604 | BAA01g13260 | A01 | 6294743 | G | A | upstream_gene_variant | MODIFIER | c.-4661C>T| |
S165 |
| 17605 | BAA01g13260 | A01 | 6295000 | G | A | upstream_gene_variant | MODIFIER | c.-4918C>T| |
S208 S219 |
| 17606 | BAA01g13260 | A01 | 6295062 | C | G | upstream_gene_variant | MODIFIER | c.-4980G>C| |
S191 |
| 17607 | BAA01g13290 | A01 | 6296045 | C | T | upstream_gene_variant | MODIFIER | c.-162C>T| |
S128 |
| 17608 | BAA01g13290 | A01 | 6296240 | G | A | missense_variant | MODERATE | c.34G>A|p.Asp12Asn |
S238 |
| 17609 | BAA01g13290 | A01 | 6296454 | C | T | missense_variant | MODERATE | c.248C>T|p.Thr83Ile |
S150 |
| 17610 | BAA01g13290 | A01 | 6297001 | G | A | missense_variant | MODERATE | c.434G>A|p.Ser145Asn |
S140 S168 S219 S72 |
| 17611 | BAA01g13290 | A01 | 6297201 | G | A | missense_variant | MODERATE | c.517G>A|p.Glu173Lys |
S121 |
| 17612 | BAA01g13300 | A01 | 6297324 | G | A | upstream_gene_variant | MODIFIER | c.-1205G>A| |
S236 |
| 17613 | BAA01g13300 | A01 | 6298395 | C | T | upstream_gene_variant | MODIFIER | c.-134C>T| |
S213 |
| 17614 | BAA01g13300 | A01 | 6298692 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.77-1G>A| |
S294 |
| 17615 | BAA01g13300 | A01 | 6298701 | G | A | missense_variant | MODERATE | c.85G>A|p.Val29Met |
S298 |
| 17616 | BAA01g13300 | A01 | 6299216 | G | A | synonymous_variant | LOW | c.450G>A|p.Lys150Lys |
S240 |
| 17617 | BAA01g13300 | A01 | 6300141 | G | A | missense_variant | MODERATE | c.974G>A|p.Gly325Glu |
S117 |
| 17618 | BAA01g13290 | A01 | 6300630 | C | T | downstream_gene_variant | MODIFIER | c.*2645C>T| |
S139 |
| 17619 | BAA01g13310 | A01 | 6302023 | G | A | missense_variant | MODERATE | c.637C>T|p.Leu213Phe |
S105 S106 |
| 17620 | BAA01g13290 | A01 | 6302219 | G | A | downstream_gene_variant | MODIFIER | c.*4234G>A| |
S256 |
| 17621 | BAA01g13310 | A01 | 6302772 | C | T | missense_variant | MODERATE | c.368G>A|p.Gly123Glu |
S260 |
| 17622 | BAA01g13310 | A01 | 6303951 | G | A | upstream_gene_variant | MODIFIER | c.-713C>T| |
S244 |
| 17623 | BAA01g13310 | A01 | 6304517 | G | A | upstream_gene_variant | MODIFIER | c.-1279C>T| |
S209 |
| 17624 | BAA01g13310 | A01 | 6305128 | C | T | upstream_gene_variant | MODIFIER | c.-1890G>A| |
S69 |
| 17625 | BAA01g13310 | A01 | 6305929 | C | T | upstream_gene_variant | MODIFIER | c.-2691G>A| |
S289 S290 |