| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 31601 | BAA01g21900 | A01 | 10905832 | G | A | upstream_gene_variant | MODIFIER | c.-4400C>T| |
S32 |
| 31602 | BAA01g21910 | A01 | 10906659 | A | C | downstream_gene_variant | MODIFIER | c.*2244T>G| |
S20 |
| 31603 | BAA01g21910 | A01 | 10907241 | G | A | downstream_gene_variant | MODIFIER | c.*1662C>T| |
S157 |
| 31604 | BAA01g21910 | A01 | 10907537 | G | A | downstream_gene_variant | MODIFIER | c.*1366C>T| |
S129 |
| 31605 | BAA01g21910 | A01 | 10907553 | G | T | downstream_gene_variant | MODIFIER | c.*1350C>A| |
S19 |
| 31606 | BAA01g21910 | A01 | 10907911 | C | T | downstream_gene_variant | MODIFIER | c.*992G>A| |
S215 |
| 31607 | BAA01g21910 | A01 | 10908284 | G | A | downstream_gene_variant | MODIFIER | c.*619C>T| |
S37 |
| 31608 | BAA01g21910 | A01 | 10908979 | C | T | missense_variant | MODERATE | c.1007G>A|p.Arg336Gln |
S289 S290 |
| 31609 | BAA01g21910 | A01 | 10911014 | G | A | missense_variant | MODERATE | c.229C>T|p.Pro77Ser |
S58 |
| 31610 | BAA01g21920 | A01 | 10914272 | C | T | missense_variant | MODERATE | c.247G>A|p.Val83Met |
S77 S82 |
| 31611 | BAA01g21920 | A01 | 10914391 | G | A | missense_variant | MODERATE | c.128C>T|p.Ser43Phe |
S268 |
| 31612 | BAA01g21910 | A01 | 10914545 | G | A | upstream_gene_variant | MODIFIER | c.-3303C>T| |
S114 |
| 31613 | BAA01g21910 | A01 | 10914560 | C | T | upstream_gene_variant | MODIFIER | c.-3318G>A| |
S208 |
| 31614 | BAA01g21910 | A01 | 10914605 | G | A | upstream_gene_variant | MODIFIER | c.-3363C>T| |
S159 S243 |
| 31615 | BAA01g21910 | A01 | 10915789 | G | A | upstream_gene_variant | MODIFIER | c.-4547C>T| |
S163 |
| 31616 | BAA01g21920 | A01 | 10917986 | C | T | upstream_gene_variant | MODIFIER | c.-3468G>A| |
S46 |
| 31617 | BAA01g21940 | A01 | 10918041 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.328-1G>A| |
S287 |
| 31618 | BAA01g21940 | A01 | 10919080 | C | T | missense_variant | MODERATE | c.823C>T|p.Leu275Phe |
S38 |
| 31619 | BAA01g21930 | A01 | 10919695 | C | T | downstream_gene_variant | MODIFIER | c.*3239C>T| |
S237 |
| 31620 | BAA01g21930 | A01 | 10919715 | G | A | downstream_gene_variant | MODIFIER | c.*3259G>A| |
S56 |
| 31621 | BAA01g21940 | A01 | 10920068 | C | T | missense_variant | MODERATE | c.1214C>T|p.Pro405Leu |
S134 |
| 31622 | BAA01g21930 | A01 | 10920326 | C | T | downstream_gene_variant | MODIFIER | c.*3870C>T| |
S161 S228 S244 S289 S290 |
| 31623 | BAA01g21930 | A01 | 10920362 | C | T | downstream_gene_variant | MODIFIER | c.*3906C>T| |
S228 |
| 31624 | BAA01g21940 | A01 | 10920411 | C | T | splice_region_variant&intron_variant | LOW | c.1321-4C>T| |
S182 |
| 31625 | BAA01g21930 | A01 | 10921108 | C | T | downstream_gene_variant | MODIFIER | c.*4652C>T| |
S10 |