| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 44451 | BAA01g26940 | A01 | 15232179 | C | T | upstream_gene_variant | MODIFIER | c.-375C>T| |
S282 |
| 44452 | BAA01g26940 | A01 | 15232386 | C | T | upstream_gene_variant | MODIFIER | c.-168C>T| |
S286 |
| 44453 | BAA01g26960 | A01 | 15234624 | G | A | upstream_gene_variant | MODIFIER | c.-4429G>A| |
S12 |
| 44454 | BAA01g26950 | A01 | 15235464 | C | T | missense_variant | MODERATE | c.209G>A|p.Gly70Glu |
S99 |
| 44455 | BAA01g26950 | A01 | 15235518 | G | A | missense_variant | MODERATE | c.155C>T|p.Ala52Val |
S116 |
| 44456 | BAA01g26950 | A01 | 15235547 | C | T | synonymous_variant | LOW | c.126G>A|p.Pro42Pro |
S81 S85 |
| 44457 | BAA01g26950 | A01 | 15235637 | G | A | synonymous_variant | LOW | c.36C>T|p.Asp12Asp |
S105 S106 |
| 44458 | BAA01g26950 | A01 | 15235871 | C | T | upstream_gene_variant | MODIFIER | c.-199G>A| |
S11 |
| 44459 | BAA01g26950 | A01 | 15236767 | G | A | upstream_gene_variant | MODIFIER | c.-1095C>T| |
S32 |
| 44460 | BAA01g26950 | A01 | 15236872 | C | T | upstream_gene_variant | MODIFIER | c.-1200G>A| |
S303 |
| 44461 | BAA01g26950 | A01 | 15238516 | C | T | upstream_gene_variant | MODIFIER | c.-2844G>A| |
S166 |
| 44462 | BAA01g26950 | A01 | 15239390 | G | A | upstream_gene_variant | MODIFIER | c.-3718C>T| |
S172 S217 |
| 44463 | BAA01g26950 | A01 | 15240365 | G | A | upstream_gene_variant | MODIFIER | c.-4693C>T| |
S84 S93 |
| 44464 | BAA01g26960 | A01 | 15240834 | C | T | downstream_gene_variant | MODIFIER | c.*1076C>T| |
S135 |
| 44465 | BAA01g26960 | A01 | 15240979 | C | T | downstream_gene_variant | MODIFIER | c.*1221C>T| |
S162 |
| 44466 | BAA01g26960 | A01 | 15241139 | C | T | downstream_gene_variant | MODIFIER | c.*1381C>T| |
S136 |
| 44467 | BAA01g26960 | A01 | 15241312 | C | T | downstream_gene_variant | MODIFIER | c.*1554C>T| |
S20 |
| 44468 | BAA01g26960 | A01 | 15241686 | G | A | downstream_gene_variant | MODIFIER | c.*1928G>A| |
S292 |
| 44469 | BAA01g26960 | A01 | 15241688 | G | A | downstream_gene_variant | MODIFIER | c.*1930G>A| |
S288 |
| 44470 | BAA01g26970 | A01 | 15244308 | C | T | missense_variant&splice_region_variant | MODERATE | c.3067G>A|p.Gly1023Arg |
S99 |
| 44471 | BAA01g26970 | A01 | 15244362 | G | A | stop_gained | HIGH | c.3013C>T|p.Gln1005* |
S197 |
| 44472 | BAA01g26970 | A01 | 15245180 | C | T | missense_variant | MODERATE | c.2492G>A|p.Arg831Lys |
S20 |
| 44473 | BAA01g26970 | A01 | 15248452 | G | A | missense_variant | MODERATE | c.1423C>T|p.His475Tyr |
S23 |
| 44474 | BAA01g26970 | A01 | 15249672 | C | T | synonymous_variant | LOW | c.369G>A|p.Glu123Glu |
S132 S137 S215 |
| 44475 | BAA01g26970 | A01 | 15249870 | C | T | missense_variant | MODERATE | c.275G>A|p.Gly92Glu |
S120 |