| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 66651 | BAA01g34900 | A01 | 23323478 | C | T | upstream_gene_variant | MODIFIER | c.-1923G>A| |
S167 |
| 66652 | BAA01g34900 | A01 | 23323929 | C | T | upstream_gene_variant | MODIFIER | c.-2374G>A| |
S178 |
| 66653 | BAA01g34900 | A01 | 23325758 | G | A | upstream_gene_variant | MODIFIER | c.-4203C>T| |
S252 |
| 66654 | BAA01g34900 | A01 | 23326151 | C | T | upstream_gene_variant | MODIFIER | c.-4596G>A| |
S112 |
| 66655 | BAA01g34900 | A01 | 23326187 | G | A | upstream_gene_variant | MODIFIER | c.-4632C>T| |
S65 |
| 66656 | BAA01g34910 | A01 | 23327423 | C | T | downstream_gene_variant | MODIFIER | c.*4743G>A| |
S251 |
| 66657 | BAA01g34910 | A01 | 23327460 | G | A | downstream_gene_variant | MODIFIER | c.*4706C>T| |
S207 |
| 66658 | BAA01g34910 | A01 | 23327484 | C | T | downstream_gene_variant | MODIFIER | c.*4682G>A| |
S293 |
| 66659 | BAA01g34910 | A01 | 23327642 | C | T | downstream_gene_variant | MODIFIER | c.*4524G>A| |
S42 |
| 66660 | BAA01g34910 | A01 | 23327725 | C | T | downstream_gene_variant | MODIFIER | c.*4441G>A| |
S249 |
| 66661 | BAA01g34910 | A01 | 23327938 | C | T | downstream_gene_variant | MODIFIER | c.*4228G>A| |
S119 |
| 66662 | BAA01g34910 | A01 | 23328270 | C | T | downstream_gene_variant | MODIFIER | c.*3896G>A| |
S272 |
| 66663 | BAA01g34910 | A01 | 23328384 | C | T | downstream_gene_variant | MODIFIER | c.*3782G>A| |
S194 |
| 66664 | BAA01g34910 | A01 | 23328387 | C | T | downstream_gene_variant | MODIFIER | c.*3779G>A| |
S51 |
| 66665 | BAA01g34910 | A01 | 23328696 | G | A | downstream_gene_variant | MODIFIER | c.*3470C>T| |
S246 |
| 66666 | BAA01g34910 | A01 | 23328799 | C | T | downstream_gene_variant | MODIFIER | c.*3367G>A| |
S82 S92 |
| 66667 | BAA01g34910 | A01 | 23329013 | G | A | downstream_gene_variant | MODIFIER | c.*3153C>T| |
S281 |
| 66668 | BAA01g34910 | A01 | 23331185 | G | A | downstream_gene_variant | MODIFIER | c.*981C>T| |
S297 |
| 66669 | BAA01g34910 | A01 | 23332618 | C | T | intron_variant | MODIFIER | c.588+174G>A| |
S249 |
| 66670 | BAA01g34910 | A01 | 23332976 | G | A | missense_variant | MODERATE | c.475C>T|p.Leu159Phe |
S299 |
| 66671 | BAA01g34910 | A01 | 23336499 | G | A | upstream_gene_variant | MODIFIER | c.-2911C>T| |
S157 S163 |
| 66672 | BAA01g34910-BAA01g34920 | A01 | 23338910 | C | T | intergenic_region | MODIFIER | n.23338910C>T| |
S192 |
| 66673 | BAA01g34910-BAA01g34920 | A01 | 23339006 | C | T | intergenic_region | MODIFIER | n.23339006C>T| |
S205 |
| 66674 | BAA01g34910-BAA01g34920 | A01 | 23342126 | G | A | intergenic_region | MODIFIER | n.23342126G>A| |
S260 |
| 66675 | BAA01g34920 | A01 | 23349654 | C | T | downstream_gene_variant | MODIFIER | c.*3786G>A| |
S182 |