| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 78351 | BAA01g41200 | A01 | 27401317 | G | A | missense_variant | MODERATE | c.101G>A|p.Cys34Tyr |
S221 |
| 78352 | BAA01g41200 | A01 | 27401443 | C | T | splice_region_variant&intron_variant | LOW | c.219+8C>T| |
S183 S198 |
| 78353 | BAA01g41190 | A01 | 27402420 | C | T | downstream_gene_variant | MODIFIER | c.*3197C>T| |
S303 |
| 78354 | BAA01g41210 | A01 | 27403780 | C | T | splice_donor_variant&intron_variant | HIGH | c.340+1G>A| |
S183 |
| 78355 | BAA01g41210 | A01 | 27405319 | C | T | upstream_gene_variant | MODIFIER | c.-589G>A| |
S242 |
| 78356 | BAA01g41210 | A01 | 27405394 | G | A | upstream_gene_variant | MODIFIER | c.-664C>T| |
S76 |
| 78357 | BAA01g41210 | A01 | 27406366 | G | A | upstream_gene_variant | MODIFIER | c.-1636C>T| |
S229 |
| 78358 | BAA01g41210 | A01 | 27406726 | C | T | upstream_gene_variant | MODIFIER | c.-1996G>A| |
S288 |
| 78359 | BAA01g41210 | A01 | 27407257 | G | A | upstream_gene_variant | MODIFIER | c.-2527C>T| |
S232 |
| 78360 | BAA01g41210 | A01 | 27407262 | C | T | upstream_gene_variant | MODIFIER | c.-2532G>A| |
S25 |
| 78361 | BAA01g41210 | A01 | 27407394 | C | T | upstream_gene_variant | MODIFIER | c.-2664G>A| |
S279 |
| 78362 | BAA01g41210 | A01 | 27407653 | C | T | upstream_gene_variant | MODIFIER | c.-2923G>A| |
S169 |
| 78363 | BAA01g41210 | A01 | 27409234 | G | A | upstream_gene_variant | MODIFIER | c.-4504C>T| |
S197 |
| 78364 | BAA01g41220 | A01 | 27410335 | C | T | intron_variant | MODIFIER | c.181-369C>T| |
S59 |
| 78365 | BAA01g41220 | A01 | 27410403 | G | A | intron_variant | MODIFIER | c.181-301G>A| |
S245 |
| 78366 | BAA01g41220 | A01 | 27410741 | C | T | missense_variant | MODERATE | c.218C>T|p.Ser73Leu |
S174 S27 |
| 78367 | BAA01g41220 | A01 | 27410822 | C | T | intron_variant | MODIFIER | c.250-27C>T| |
S251 |
| 78368 | BAA01g41220 | A01 | 27412059 | C | T | intron_variant | MODIFIER | c.549+719C>T| |
S82 S92 |
| 78369 | BAA01g41220 | A01 | 27412626 | C | T | intron_variant | MODIFIER | c.550-705C>T| |
S247 |
| 78370 | BAA01g41220 | A01 | 27413013 | C | T | intron_variant | MODIFIER | c.550-318C>T| |
S240 |
| 78371 | BAA01g41220 | A01 | 27413339 | G | A | synonymous_variant | LOW | c.558G>A|p.Arg186Arg |
S244 |
| 78372 | BAA01g41220 | A01 | 27413873 | C | T | missense_variant | MODERATE | c.901C>T|p.Leu301Phe |
S118 |
| 78373 | BAA01g41220 | A01 | 27414071 | G | A | stop_gained | HIGH | c.1002G>A|p.Trp334* |
S173 |
| 78374 | BAA01g41220 | A01 | 27414882 | G | A | downstream_gene_variant | MODIFIER | c.*468G>A| |
S35 |
| 78375 | BAA01g41220 | A01 | 27415595 | G | A | downstream_gene_variant | MODIFIER | c.*1181G>A| |
S287 |