| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 178651 | BAA02g19490 | A02 | 10115002 | G | A | upstream_gene_variant | MODIFIER | c.-1564G>A| |
S41 |
| 178652 | BAA02g19490 | A02 | 10115830 | G | A | upstream_gene_variant | MODIFIER | c.-736G>A| |
S161 |
| 178653 | BAA02g19490 | A02 | 10116197 | C | T | upstream_gene_variant | MODIFIER | c.-369C>T| |
S275 |
| 178654 | BAA02g19490 | A02 | 10116748 | G | A | synonymous_variant | LOW | c.93G>A|p.Lys31Lys |
S129 |
| 178655 | BAA02g19490 | A02 | 10117512 | G | A | missense_variant | MODERATE | c.508G>A|p.Glu170Lys |
S33 |
| 178656 | BAA02g19500 | A02 | 10118367 | C | T | upstream_gene_variant | MODIFIER | c.-4476C>T| |
S130 |
| 178657 | BAA02g19500 | A02 | 10121604 | G | A | upstream_gene_variant | MODIFIER | c.-1239G>A| |
S293 |
| 178658 | BAA02g19500 | A02 | 10122091 | G | A | upstream_gene_variant | MODIFIER | c.-752G>A| |
S229 |
| 178659 | BAA02g19500 | A02 | 10122144 | C | T | upstream_gene_variant | MODIFIER | c.-699C>T| |
S73 S91 |
| 178660 | BAA02g19500 | A02 | 10123284 | G | A | downstream_gene_variant | MODIFIER | c.*238G>A| |
S34 |
| 178661 | BAA02g19500 | A02 | 10123695 | C | T | downstream_gene_variant | MODIFIER | c.*649C>T| |
S165 |
| 178662 | BAA02g19510 | A02 | 10125644 | C | T | upstream_gene_variant | MODIFIER | c.-1047G>A| |
S58 |
| 178663 | BAA02g19510 | A02 | 10128625 | C | T | upstream_gene_variant | MODIFIER | c.-4028G>A| |
S130 |
| 178664 | BAA02g19510 | A02 | 10128886 | C | T | upstream_gene_variant | MODIFIER | c.-4289G>A| |
S105 S106 |
| 178665 | BAA02g19510-BAA02g19520 | A02 | 10131098 | C | T | intergenic_region | MODIFIER | n.10131098C>T| |
S289 S290 |
| 178666 | BAA02g19520 | A02 | 10132560 | C | T | upstream_gene_variant | MODIFIER | c.-4314C>T| |
S221 |
| 178667 | BAA02g19520 | A02 | 10132564 | C | T | upstream_gene_variant | MODIFIER | c.-4310C>T| |
S38 |
| 178668 | BAA02g19520 | A02 | 10132643 | C | T | upstream_gene_variant | MODIFIER | c.-4231C>T| |
S71 |
| 178669 | BAA02g19520 | A02 | 10132657 | C | T | upstream_gene_variant | MODIFIER | c.-4217C>T| |
S289 S290 |
| 178670 | BAA02g19520 | A02 | 10133786 | C | T | upstream_gene_variant | MODIFIER | c.-3088C>T| |
S112 |
| 178671 | BAA02g19520 | A02 | 10136922 | G | A | missense_variant | MODERATE | c.49G>A|p.Glu17Lys |
S50 |
| 178672 | BAA02g19530 | A02 | 10137459 | G | A | upstream_gene_variant | MODIFIER | c.-3422G>A| |
S203 |
| 178673 | BAA02g19530 | A02 | 10137759 | G | A | upstream_gene_variant | MODIFIER | c.-3122G>A| |
S126 |
| 178674 | BAA02g19530 | A02 | 10138946 | G | A | upstream_gene_variant | MODIFIER | c.-1935G>A| |
S13 |
| 178675 | BAA02g19530 | A02 | 10140666 | G | A | upstream_gene_variant | MODIFIER | c.-215G>A| |
S110 |