| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 176001 | BAA02g18150 | A02 | 9147644 | C | T | stop_gained | HIGH | c.120G>A|p.Trp40* |
S194 |
| 176002 | BAA02g18150 | A02 | 9147844 | G | A | upstream_gene_variant | MODIFIER | c.-81C>T| |
S136 |
| 176003 | BAA02g18150 | A02 | 9148797 | G | A | upstream_gene_variant | MODIFIER | c.-1034C>T| |
S139 |
| 176004 | BAA02g18150 | A02 | 9149960 | G | A | upstream_gene_variant | MODIFIER | c.-2197C>T| |
S264 |
| 176005 | BAA02g18150 | A02 | 9150487 | A | G | upstream_gene_variant | MODIFIER | c.-2724T>C| |
S134 |
| 176006 | BAA02g18150 | A02 | 9150966 | C | T | upstream_gene_variant | MODIFIER | c.-3203G>A| |
S77 S82 |
| 176007 | BAA02g18150 | A02 | 9151899 | C | T | upstream_gene_variant | MODIFIER | c.-4136G>A| |
S167 |
| 176008 | BAA02g18150 | A02 | 9152760 | C | T | upstream_gene_variant | MODIFIER | c.-4997G>A| |
S9 |
| 176009 | BAA02g18170 | A02 | 9152975 | C | T | downstream_gene_variant | MODIFIER | c.*2852G>A| |
S18 |
| 176010 | BAA02g18170 | A02 | 9153152 | C | T | downstream_gene_variant | MODIFIER | c.*2675G>A| |
S77 S82 |
| 176011 | BAA02g18170 | A02 | 9153350 | G | A | downstream_gene_variant | MODIFIER | c.*2477C>T| |
S274 |
| 176012 | BAA02g18170 | A02 | 9153957 | G | A | downstream_gene_variant | MODIFIER | c.*1870C>T| |
S224 |
| 176013 | BAA02g18160 | A02 | 9154083 | C | T | missense_variant | MODERATE | c.538G>A|p.Asp180Asn |
S177 |
| 176014 | BAA02g18170 | A02 | 9154345 | G | A | downstream_gene_variant | MODIFIER | c.*1482C>T| |
S287 |
| 176015 | BAA02g18160 | A02 | 9154424 | G | A | missense_variant | MODERATE | c.401C>T|p.Ser134Phe |
S204 |
| 176016 | BAA02g18160 | A02 | 9154443 | C | T | missense_variant | MODERATE | c.382G>A|p.Gly128Arg |
S124 |
| 176017 | BAA02g18160 | A02 | 9154880 | C | T | missense_variant | MODERATE | c.85G>A|p.Glu29Lys |
S284 |
| 176018 | BAA02g18160 | A02 | 9155045 | G | A | upstream_gene_variant | MODIFIER | c.-81C>T| |
S109 S288 |
| 176019 | BAA02g18160 | A02 | 9155426 | C | T | upstream_gene_variant | MODIFIER | c.-462G>A| |
S308 |
| 176020 | BAA02g18170 | A02 | 9156004 | C | T | splice_region_variant&synonymous_variant | LOW | c.471G>A|p.Lys157Lys |
S112 |
| 176021 | BAA02g18180 | A02 | 9157182 | G | A | missense_variant | MODERATE | c.1142C>T|p.Ser381Phe |
S257 |
| 176022 | BAA02g18160 | A02 | 9157634 | G | A | upstream_gene_variant | MODIFIER | c.-2670C>T| |
S172 S217 |
| 176023 | BAA02g18160 | A02 | 9158236 | C | T | upstream_gene_variant | MODIFIER | c.-3272G>A| |
S185 |
| 176024 | BAA02g18160 | A02 | 9159803 | C | T | upstream_gene_variant | MODIFIER | c.-4839G>A| |
S301 S304 |
| 176025 | BAA02g18160 | A02 | 9159804 | G | A | upstream_gene_variant | MODIFIER | c.-4840C>T| |
S95 |