| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 42201 | BAA01g26190 | A01 | 14535150 | C | T | missense_variant | MODERATE | c.541G>A|p.Val181Met |
S270 |
| 42202 | BAA01g26190 | A01 | 14535336 | G | A | missense_variant | MODERATE | c.355C>T|p.Pro119Ser |
S169 |
| 42203 | BAA01g26190 | A01 | 14535421 | G | T | missense_variant | MODERATE | c.270C>A|p.Asn90Lys |
S241 |
| 42204 | BAA01g26190 | A01 | 14535458 | C | T | stop_gained | HIGH | c.233G>A|p.Trp78* |
S79 S84 |
| 42205 | BAA01g26190 | A01 | 14535925 | G | A | upstream_gene_variant | MODIFIER | c.-8C>T| |
S299 |
| 42206 | BAA01g26190 | A01 | 14536172 | C | T | upstream_gene_variant | MODIFIER | c.-255G>A| |
S270 |
| 42207 | BAA01g26190 | A01 | 14536249 | G | A | upstream_gene_variant | MODIFIER | c.-332C>T| |
S238 |
| 42208 | BAA01g26190 | A01 | 14536613 | C | T | upstream_gene_variant | MODIFIER | c.-696G>A| |
S35 |
| 42209 | BAA01g26190 | A01 | 14537430 | G | A | upstream_gene_variant | MODIFIER | c.-1513C>T| |
S140 |
| 42210 | BAA01g26190 | A01 | 14538880 | C | T | upstream_gene_variant | MODIFIER | c.-2963G>A| |
S82 S92 |
| 42211 | BAA01g26190 | A01 | 14539228 | G | A | upstream_gene_variant | MODIFIER | c.-3311C>T| |
S198 |
| 42212 | BAA01g26190 | A01 | 14539263 | G | A | upstream_gene_variant | MODIFIER | c.-3346C>T| |
S197 |
| 42213 | BAA01g26190 | A01 | 14539576 | C | T | upstream_gene_variant | MODIFIER | c.-3659G>A| |
S223 |
| 42214 | BAA01g26200 | A01 | 14540079 | G | A | missense_variant | MODERATE | c.371G>A|p.Gly124Glu |
S247 |
| 42215 | BAA01g26200 | A01 | 14540540 | C | T | synonymous_variant | LOW | c.832C>T|p.Leu278Leu |
S242 |
| 42216 | BAA01g26190 | A01 | 14540866 | G | A | upstream_gene_variant | MODIFIER | c.-4949C>T| |
S263 |
| 42217 | BAA01g26200 | A01 | 14541369 | G | A | downstream_gene_variant | MODIFIER | c.*459G>A| |
S139 |
| 42218 | BAA01g26200 | A01 | 14541534 | C | T | downstream_gene_variant | MODIFIER | c.*624C>T| |
S20 |
| 42219 | BAA01g26200 | A01 | 14541666 | G | A | downstream_gene_variant | MODIFIER | c.*756G>A| |
S92 |
| 42220 | BAA01g26200 | A01 | 14541909 | G | A | downstream_gene_variant | MODIFIER | c.*999G>A| |
S126 |
| 42221 | BAA01g26200 | A01 | 14542695 | G | A | downstream_gene_variant | MODIFIER | c.*1785G>A| |
S195 |
| 42222 | BAA01g26200 | A01 | 14543037 | C | T | downstream_gene_variant | MODIFIER | c.*2127C>T| |
S19 |
| 42223 | BAA01g26200 | A01 | 14543245 | G | A | downstream_gene_variant | MODIFIER | c.*2335G>A| |
S58 |
| 42224 | BAA01g26200 | A01 | 14543744 | G | A | downstream_gene_variant | MODIFIER | c.*2834G>A| |
S6 |
| 42225 | BAA01g26200 | A01 | 14544425 | G | A | downstream_gene_variant | MODIFIER | c.*3515G>A| |
S274 |