| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 20601 | BAA01g15180 | A01 | 7271058 | C | T | downstream_gene_variant | MODIFIER | c.*1041C>T| |
S267 |
| 20602 | BAA01g15180 | A01 | 7271899 | C | T | downstream_gene_variant | MODIFIER | c.*1882C>T| |
S43 |
| 20603 | BAA01g15180 | A01 | 7272172 | G | A | downstream_gene_variant | MODIFIER | c.*2155G>A| |
S238 |
| 20604 | BAA01g15180 | A01 | 7273621 | C | T | downstream_gene_variant | MODIFIER | c.*3604C>T| |
S1 S90 |
| 20605 | BAA01g15180 | A01 | 7273849 | G | A | downstream_gene_variant | MODIFIER | c.*3832G>A| |
S131 |
| 20606 | BAA01g15180 | A01 | 7274562 | G | C | downstream_gene_variant | MODIFIER | c.*4545G>C| |
|
| 20607 | BAA01g15180-BAA01g15190 | A01 | 7275685 | G | A | intergenic_region | MODIFIER | n.7275685G>A| |
S149 |
| 20608 | BAA01g15180-BAA01g15190 | A01 | 7276455 | C | T | intergenic_region | MODIFIER | n.7276455C>T| |
S176 |
| 20609 | BAA01g15180-BAA01g15190 | A01 | 7276472 | G | A | intergenic_region | MODIFIER | n.7276472G>A| |
S86 |
| 20610 | BAA01g15180-BAA01g15190 | A01 | 7276940 | A | G | intergenic_region | MODIFIER | n.7276940A>G| |
S280 |
| 20611 | BAA01g15190 | A01 | 7279597 | C | T | upstream_gene_variant | MODIFIER | c.-3188C>T| |
S10 |
| 20612 | BAA01g15190 | A01 | 7279848 | C | T | upstream_gene_variant | MODIFIER | c.-2937C>T| |
S247 |
| 20613 | BAA01g15190 | A01 | 7279959 | G | A | upstream_gene_variant | MODIFIER | c.-2826G>A| |
S133 |
| 20614 | BAA01g15190 | A01 | 7280873 | C | T | upstream_gene_variant | MODIFIER | c.-1912C>T| |
S249 |
| 20615 | BAA01g15190 | A01 | 7281518 | G | A | upstream_gene_variant | MODIFIER | c.-1267G>A| |
S174 S216 S241 S27 S39 |
| 20616 | BAA01g15190 | A01 | 7282507 | G | A | upstream_gene_variant | MODIFIER | c.-278G>A| |
S238 |
| 20617 | BAA01g15190 | A01 | 7282980 | G | A | missense_variant | MODERATE | c.196G>A|p.Asp66Asn |
S142 |
| 20618 | BAA01g15190 | A01 | 7283268 | C | T | missense_variant | MODERATE | c.484C>T|p.Pro162Ser |
S159 S243 |
| 20619 | BAA01g15190 | A01 | 7283774 | G | A | missense_variant | MODERATE | c.755G>A|p.Gly252Asp |
S9 |
| 20620 | BAA01g15190 | A01 | 7283990 | G | A | stop_gained&splice_region_variant | HIGH | c.813G>A|p.Trp271* |
S229 |
| 20621 | BAA01g15200 | A01 | 7284699 | T | C | upstream_gene_variant | MODIFIER | c.-1648T>C| |
S169 |
| 20622 | BAA01g15200 | A01 | 7284969 | C | T | upstream_gene_variant | MODIFIER | c.-1378C>T| |
S264 |
| 20623 | BAA01g15190 | A01 | 7286497 | C | T | downstream_gene_variant | MODIFIER | c.*2471C>T| |
S63 |
| 20624 | BAA01g15190 | A01 | 7287009 | G | A | downstream_gene_variant | MODIFIER | c.*2983G>A| |
S209 |
| 20625 | BAA01g15190 | A01 | 7287931 | C | T | downstream_gene_variant | MODIFIER | c.*3905C>T| |
S148 S30 S31 |