| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 169751 | BAA02g14760 | A02 | 6960635 | C | T | upstream_gene_variant | MODIFIER | c.-3999G>A| |
S272 |
| 169752 | BAA02g14760 | A02 | 6961553 | G | A | upstream_gene_variant | MODIFIER | c.-4917C>T| |
S48 |
| 169753 | BAA02g14760 | A02 | 6961602 | G | A | upstream_gene_variant | MODIFIER | c.-4966C>T| |
S188 |
| 169754 | BAA02g14770 | A02 | 6963947 | G | A | upstream_gene_variant | MODIFIER | c.-2963G>A| |
S125 |
| 169755 | BAA02g14780 | A02 | 6969118 | G | A | upstream_gene_variant | MODIFIER | c.-4158G>A| |
S202 |
| 169756 | BAA02g14780 | A02 | 6969348 | C | T | upstream_gene_variant | MODIFIER | c.-3928C>T| |
S210 |
| 169757 | BAA02g14780 | A02 | 6969717 | C | T | upstream_gene_variant | MODIFIER | c.-3559C>T| |
S44 |
| 169758 | BAA02g14780 | A02 | 6969752 | C | T | upstream_gene_variant | MODIFIER | c.-3524C>T| |
S283 |
| 169759 | BAA02g14780 | A02 | 6969840 | G | A | upstream_gene_variant | MODIFIER | c.-3436G>A| |
S223 |
| 169760 | BAA02g14780 | A02 | 6970517 | C | T | upstream_gene_variant | MODIFIER | c.-2759C>T| |
S97 |
| 169761 | BAA02g14780 | A02 | 6971140 | G | A | upstream_gene_variant | MODIFIER | c.-2136G>A| |
S23 |
| 169762 | BAA02g14780 | A02 | 6972875 | C | T | upstream_gene_variant | MODIFIER | c.-401C>T| |
S179 |
| 169763 | BAA02g14780 | A02 | 6973063 | G | A | upstream_gene_variant | MODIFIER | c.-213G>A| |
S28 |
| 169764 | BAA02g14780 | A02 | 6973344 | C | T | synonymous_variant | LOW | c.69C>T|p.Pro23Pro |
S208 |
| 169765 | BAA02g14770 | A02 | 6973685 | T | G | downstream_gene_variant | MODIFIER | c.*4821T>G| |
S128 |
| 169766 | BAA02g14780 | A02 | 6974142 | C | T | missense_variant | MODERATE | c.245C>T|p.Pro82Leu |
S199 |
| 169767 | BAA02g14790 | A02 | 6974224 | C | T | downstream_gene_variant | MODIFIER | c.*2654G>A| |
S128 |
| 169768 | BAA02g14780 | A02 | 6974855 | G | A | missense_variant | MODERATE | c.716G>A|p.Arg239Lys |
S276 |
| 169769 | BAA02g14780 | A02 | 6976507 | C | T | downstream_gene_variant | MODIFIER | c.*612C>T| |
S233 |
| 169770 | BAA02g14790 | A02 | 6976961 | C | T | missense_variant | MODERATE | c.967G>A|p.Val323Ile |
S211 S227 |
| 169771 | BAA02g14790 | A02 | 6977266 | C | T | synonymous_variant | LOW | c.738G>A|p.Lys246Lys |
S128 |
| 169772 | BAA02g14780 | A02 | 6978012 | G | A | downstream_gene_variant | MODIFIER | c.*2117G>A| |
S198 |
| 169773 | BAA02g14790 | A02 | 6979421 | C | T | upstream_gene_variant | MODIFIER | c.-717G>A| |
S180 |
| 169774 | BAA02g14790 | A02 | 6979512 | C | T | upstream_gene_variant | MODIFIER | c.-808G>A| |
S16 |
| 169775 | BAA02g14790 | A02 | 6979891 | G | A | upstream_gene_variant | MODIFIER | c.-1187C>T| |
S148 S30 S31 |