| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 165651 | BAA02g11840 | A02 | 5349691 | G | A | upstream_gene_variant | MODIFIER | c.-475C>T| |
S173 |
| 165652 | BAA02g11840 | A02 | 5350191 | C | T | upstream_gene_variant | MODIFIER | c.-975G>A| |
S142 |
| 165653 | BAA02g11850 | A02 | 5350887 | C | T | missense_variant | MODERATE | c.215C>T|p.Ser72Phe |
S77 S82 |
| 165654 | BAA02g11850 | A02 | 5351021 | G | A | missense_variant | MODERATE | c.259G>A|p.Asp87Asn |
S247 |
| 165655 | BAA02g11840 | A02 | 5351082 | C | T | upstream_gene_variant | MODIFIER | c.-1866G>A| |
S183 S198 |
| 165656 | BAA02g11860 | A02 | 5352838 | C | T | synonymous_variant | LOW | c.552G>A|p.Glu184Glu |
S266 |
| 165657 | BAA02g11860 | A02 | 5352872 | G | A | missense_variant | MODERATE | c.518C>T|p.Pro173Leu |
S137 S215 |
| 165658 | BAA02g11860 | A02 | 5353457 | C | T | missense_variant | MODERATE | c.250G>A|p.Asp84Asn |
S250 |
| 165659 | BAA02g11860 | A02 | 5353579 | A | C | missense_variant | MODERATE | c.128T>G|p.Leu43Arg |
S107 S111 S115 S13 S144 S149 S17 S198 S236 S242 S252 S261 S295 S35 S73 S78 |
| 165660 | BAA02g11860 | A02 | 5353595 | C | G | missense_variant | MODERATE | c.112G>C|p.Ala38Pro |
S10 S111 S176 S246 S257 S278 S295 |
| 165661 | BAA02g11840 | A02 | 5353893 | G | A | upstream_gene_variant | MODIFIER | c.-4677C>T| |
S95 |
| 165662 | BAA02g11840 | A02 | 5354012 | C | T | upstream_gene_variant | MODIFIER | c.-4796G>A| |
S185 |
| 165663 | BAA02g11870 | A02 | 5355238 | C | T | missense_variant | MODERATE | c.493G>A|p.Val165Ile |
S289 S290 |
| 165664 | BAA02g11860 | A02 | 5356722 | C | T | upstream_gene_variant | MODIFIER | c.-3016G>A| |
S121 |
| 165665 | BAA02g11860 | A02 | 5356926 | C | T | upstream_gene_variant | MODIFIER | c.-3220G>A| |
S138 |
| 165666 | BAA02g11860 | A02 | 5357035 | G | A | upstream_gene_variant | MODIFIER | c.-3329C>T| |
S296 |
| 165667 | BAA02g11860 | A02 | 5358326 | C | T | upstream_gene_variant | MODIFIER | c.-4620G>A| |
S111 |
| 165668 | BAA02g11870 | A02 | 5358815 | C | T | upstream_gene_variant | MODIFIER | c.-2630G>A| |
S257 |
| 165669 | BAA02g11870 | A02 | 5359471 | G | A | upstream_gene_variant | MODIFIER | c.-3286C>T| |
S51 |
| 165670 | BAA02g11870 | A02 | 5360192 | C | T | upstream_gene_variant | MODIFIER | c.-4007G>A| |
S183 S198 |
| 165671 | BAA02g11870 | A02 | 5360206 | C | T | upstream_gene_variant | MODIFIER | c.-4021G>A| |
S120 |
| 165672 | BAA02g11870 | A02 | 5360426 | G | A | upstream_gene_variant | MODIFIER | c.-4241C>T| |
S295 |
| 165673 | BAA02g11870 | A02 | 5360563 | C | T | upstream_gene_variant | MODIFIER | c.-4378G>A| |
S299 |
| 165674 | BAA02g11870 | A02 | 5360768 | G | A | upstream_gene_variant | MODIFIER | c.-4583C>T| |
S207 |
| 165675 | BAA02g11870 | A02 | 5360999 | C | T | upstream_gene_variant | MODIFIER | c.-4814G>A| |
S128 |