| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 116301 | BAA10g10180 | A10 | 11967278 | C | T | missense_variant | MODERATE | c.755C>T|p.Pro252Leu |
S61 |
| 116302 | BAA10g10180 | A10 | 11968441 | G | A | downstream_gene_variant | MODIFIER | c.*723G>A| |
S48 |
| 116303 | BAA10g10180 | A10 | 11968530 | G | A | downstream_gene_variant | MODIFIER | c.*812G>A| |
S189 S202 |
| 116304 | BAA10g10190 | A10 | 11969050 | C | T | missense_variant | MODERATE | c.154C>T|p.Pro52Ser |
S115 |
| 116305 | BAA10g10180 | A10 | 11969563 | C | T | downstream_gene_variant | MODIFIER | c.*1845C>T| |
S298 |
| 116306 | BAA10g10180 | A10 | 11972214 | G | A | downstream_gene_variant | MODIFIER | c.*4496G>A| |
S53 |
| 116307 | BAA10g10190 | A10 | 11973408 | C | T | downstream_gene_variant | MODIFIER | c.*4176C>T| |
S249 |
| 116308 | BAA10g10200 | A10 | 11974431 | C | T | upstream_gene_variant | MODIFIER | c.-4679C>T| |
S149 |
| 116309 | BAA10g10200 | A10 | 11975200 | C | T | upstream_gene_variant | MODIFIER | c.-3910C>T| |
S133 |
| 116310 | BAA10g10200 | A10 | 11975259 | C | T | upstream_gene_variant | MODIFIER | c.-3851C>T| |
S166 |
| 116311 | BAA10g10200 | A10 | 11975761 | G | A | upstream_gene_variant | MODIFIER | c.-3349G>A| |
S283 |
| 116312 | BAA10g10200 | A10 | 11976665 | G | A | upstream_gene_variant | MODIFIER | c.-2445G>A| |
S16 |
| 116313 | BAA10g10200 | A10 | 11978188 | G | A | upstream_gene_variant | MODIFIER | c.-922G>A| |
S35 |
| 116314 | BAA10g10200 | A10 | 11979286 | C | T | intron_variant | MODIFIER | c.163+14C>T| |
S63 |
| 116315 | BAA10g10200 | A10 | 11979770 | C | T | missense_variant | MODERATE | c.472C>T|p.Arg158Cys |
S156 |
| 116316 | BAA10g10200 | A10 | 11980371 | C | T | missense_variant | MODERATE | c.1073C>T|p.Ser358Phe |
S243 S299 |
| 116317 | BAA10g10200 | A10 | 11980676 | C | T | synonymous_variant | LOW | c.1378C>T|p.Leu460Leu |
S113 |
| 116318 | BAA10g10200 | A10 | 11980704 | G | A | missense_variant | MODERATE | c.1406G>A|p.Gly469Glu |
S178 |
| 116319 | BAA10g10200 | A10 | 11980815 | G | A | downstream_gene_variant | MODIFIER | c.*17G>A| |
S118 |
| 116320 | BAA10g10200 | A10 | 11981149 | C | T | downstream_gene_variant | MODIFIER | c.*351C>T| |
S11 |
| 116321 | BAA10g10200 | A10 | 11981333 | C | T | downstream_gene_variant | MODIFIER | c.*535C>T| |
S169 |
| 116322 | BAA10g10200 | A10 | 11982514 | G | A | downstream_gene_variant | MODIFIER | c.*1716G>A| |
S179 |
| 116323 | BAA10g10200 | A10 | 11982777 | G | A | downstream_gene_variant | MODIFIER | c.*1979G>A| |
S172 S217 |
| 116324 | BAA10g10200 | A10 | 11983032 | G | A | downstream_gene_variant | MODIFIER | c.*2234G>A| |
S278 |
| 116325 | BAA10g10200 | A10 | 11983390 | G | A | downstream_gene_variant | MODIFIER | c.*2592G>A| |
S208 S219 |