| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 87451 | BAA01g46620 | A01 | 31037490 | C | T | missense_variant | MODERATE | c.376G>A|p.Glu126Lys |
S185 |
| 87452 | BAA01g46620 | A01 | 31037884 | G | A | missense_variant | MODERATE | c.163C>T|p.Leu55Phe |
S239 |
| 87453 | BAA01g46620 | A01 | 31037889 | G | A | missense_variant | MODERATE | c.158C>T|p.Ser53Phe |
S63 |
| 87454 | BAA01g46640 | A01 | 31045610 | G | A | upstream_gene_variant | MODIFIER | c.-3681G>A| |
S37 |
| 87455 | BAA01g46640 | A01 | 31045700 | C | T | upstream_gene_variant | MODIFIER | c.-3591C>T| |
S250 |
| 87456 | BAA01g46630 | A01 | 31045967 | C | T | missense_variant | MODERATE | c.427G>A|p.Glu143Lys |
S149 |
| 87457 | BAA01g46630 | A01 | 31046880 | G | A | upstream_gene_variant | MODIFIER | c.-132C>T| |
S130 |
| 87458 | BAA01g46630 | A01 | 31047225 | G | A | upstream_gene_variant | MODIFIER | c.-477C>T| |
S192 |
| 87459 | BAA01g46630 | A01 | 31047585 | G | A | upstream_gene_variant | MODIFIER | c.-837C>T| |
S273 |
| 87460 | BAA01g46630 | A01 | 31047794 | C | T | upstream_gene_variant | MODIFIER | c.-1046G>A| |
S139 |
| 87461 | BAA01g46630 | A01 | 31048999 | C | T | upstream_gene_variant | MODIFIER | c.-2251G>A| |
S173 |
| 87462 | BAA01g46630 | A01 | 31049035 | G | A | upstream_gene_variant | MODIFIER | c.-2287C>T| |
S211 S227 |
| 87463 | BAA01g46630 | A01 | 31049281 | C | T | upstream_gene_variant | MODIFIER | c.-2533G>A| |
S119 |
| 87464 | BAA01g46630 | A01 | 31049892 | G | A | upstream_gene_variant | MODIFIER | c.-3144C>T| |
S7 |
| 87465 | BAA01g46640 | A01 | 31050541 | C | T | missense_variant | MODERATE | c.745C>T|p.Pro249Ser |
S218 |
| 87466 | BAA01g46650 | A01 | 31052378 | C | T | upstream_gene_variant | MODIFIER | c.-218C>T| |
S108 |
| 87467 | BAA01g46640 | A01 | 31054255 | G | A | downstream_gene_variant | MODIFIER | c.*3266G>A| |
S225 S73 |
| 87468 | BAA01g46650 | A01 | 31054292 | C | T | missense_variant | MODERATE | c.1564C>T|p.Pro522Ser |
S91 |
| 87469 | BAA01g46650 | A01 | 31054332 | C | T | missense_variant | MODERATE | c.1604C>T|p.Pro535Leu |
S99 |
| 87470 | BAA01g46640 | A01 | 31055629 | C | T | downstream_gene_variant | MODIFIER | c.*4640C>T| |
S114 |
| 87471 | BAA01g46640 | A01 | 31055738 | C | T | downstream_gene_variant | MODIFIER | c.*4749C>T| |
S295 |
| 87472 | BAA01g46650 | A01 | 31056583 | G | A | downstream_gene_variant | MODIFIER | c.*2004G>A| |
S63 |
| 87473 | BAA01g46660 | A01 | 31058237 | G | A | upstream_gene_variant | MODIFIER | c.-1215C>T| |
S182 |
| 87474 | BAA01g46660 | A01 | 31059232 | C | T | upstream_gene_variant | MODIFIER | c.-2210G>A| |
S172 |
| 87475 | BAA01g46660 | A01 | 31059861 | G | A | upstream_gene_variant | MODIFIER | c.-2839C>T| |
S16 |