| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 182151 | BAA02g21260 | A02 | 11396352 | C | T | missense_variant | MODERATE | c.1336G>A|p.Ala446Thr |
S208 S219 |
| 182152 | BAA02g21270 | A02 | 11396758 | G | A | downstream_gene_variant | MODIFIER | c.*4906C>T| |
S259 |
| 182153 | BAA02g21260 | A02 | 11398474 | C | T | synonymous_variant | LOW | c.423G>A|p.Gly141Gly |
S211 S227 |
| 182154 | BAA02g21270 | A02 | 11399687 | A | T | downstream_gene_variant | MODIFIER | c.*1977T>A| |
S146 |
| 182155 | BAA02g21260 | A02 | 11400475 | C | T | missense_variant | MODERATE | c.80G>A|p.Arg27Gln |
S255 |
| 182156 | BAA02g21260 | A02 | 11401651 | G | A | upstream_gene_variant | MODIFIER | c.-1097C>T| |
S113 |
| 182157 | BAA02g21270 | A02 | 11401737 | G | A | missense_variant | MODERATE | c.2258C>T|p.Thr753Ile |
S303 |
| 182158 | BAA02g21270 | A02 | 11401743 | C | T | missense_variant | MODERATE | c.2252G>A|p.Arg751Lys |
S242 |
| 182159 | BAA02g21270 | A02 | 11402450 | G | A | synonymous_variant | LOW | c.1545C>T|p.Val515Val |
S95 |
| 182160 | BAA02g21270 | A02 | 11402519 | G | A | synonymous_variant | LOW | c.1476C>T|p.Phe492Phe |
S59 |
| 182161 | BAA02g21270 | A02 | 11403621 | C | T | synonymous_variant | LOW | c.951G>A|p.Gly317Gly |
S65 |
| 182162 | BAA02g21260 | A02 | 11403730 | T | C | upstream_gene_variant | MODIFIER | c.-3176A>G| |
S192 |
| 182163 | BAA02g21260 | A02 | 11403888 | G | A | upstream_gene_variant | MODIFIER | c.-3334C>T| |
S159 S243 |
| 182164 | BAA02g21260 | A02 | 11403940 | G | A | upstream_gene_variant | MODIFIER | c.-3386C>T| |
S225 S73 |
| 182165 | BAA02g21260 | A02 | 11404401 | C | T | upstream_gene_variant | MODIFIER | c.-3847G>A| |
S180 |
| 182166 | BAA02g21260 | A02 | 11404895 | C | T | upstream_gene_variant | MODIFIER | c.-4341G>A| |
S250 |
| 182167 | BAA02g21260 | A02 | 11404903 | G | A | upstream_gene_variant | MODIFIER | c.-4349C>T| |
S190 |
| 182168 | BAA02g21260 | A02 | 11405089 | G | A | upstream_gene_variant | MODIFIER | c.-4535C>T| |
S68 |
| 182169 | BAA02g21270 | A02 | 11405255 | G | A | missense_variant | MODERATE | c.431C>T|p.Thr144Met |
S296 |
| 182170 | BAA02g21270 | A02 | 11405281 | C | T | synonymous_variant | LOW | c.405G>A|p.Ser135Ser |
S135 |
| 182171 | BAA02g21270 | A02 | 11406782 | C | T | upstream_gene_variant | MODIFIER | c.-990G>A| |
S244 |
| 182172 | BAA02g21270 | A02 | 11407485 | C | T | upstream_gene_variant | MODIFIER | c.-1693G>A| |
S158 |
| 182173 | BAA02g21270 | A02 | 11408602 | C | T | upstream_gene_variant | MODIFIER | c.-2810G>A| |
S163 |
| 182174 | BAA02g21270 | A02 | 11408609 | C | T | upstream_gene_variant | MODIFIER | c.-2817G>A| |
S63 |
| 182175 | BAA02g21270 | A02 | 11409828 | C | T | upstream_gene_variant | MODIFIER | c.-4036G>A| |
S88 |