| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 174751 | BAA02g17510 | A02 | 8726425 | C | T | downstream_gene_variant | MODIFIER | c.*1511C>T| |
S161 |
| 174752 | BAA02g17510 | A02 | 8726571 | C | T | downstream_gene_variant | MODIFIER | c.*1657C>T| |
S209 |
| 174753 | BAA02g17520 | A02 | 8727942 | G | A | missense_variant | MODERATE | c.2116C>T|p.Pro706Ser |
S134 |
| 174754 | BAA02g17520 | A02 | 8728080 | C | T | missense_variant | MODERATE | c.1978G>A|p.Glu660Lys |
S303 |
| 174755 | BAA02g17520 | A02 | 8728432 | G | A | missense_variant | MODERATE | c.1961C>T|p.Pro654Leu |
S210 S225 |
| 174756 | BAA02g17520 | A02 | 8731789 | G | A | missense_variant | MODERATE | c.503C>T|p.Pro168Leu |
S67 |
| 174757 | BAA02g17520 | A02 | 8732617 | C | T | missense_variant | MODERATE | c.199G>A|p.Asp67Asn |
S183 S198 |
| 174758 | BAA02g17520 | A02 | 8733348 | G | A | upstream_gene_variant | MODIFIER | c.-533C>T| |
S170 |
| 174759 | BAA02g17520 | A02 | 8733974 | G | A | upstream_gene_variant | MODIFIER | c.-1159C>T| |
S134 |
| 174760 | BAA02g17520 | A02 | 8734044 | G | A | upstream_gene_variant | MODIFIER | c.-1229C>T| |
S187 |
| 174761 | BAA02g17520 | A02 | 8734294 | C | T | upstream_gene_variant | MODIFIER | c.-1479G>A| |
S127 |
| 174762 | BAA02g17520 | A02 | 8734438 | C | T | upstream_gene_variant | MODIFIER | c.-1623G>A| |
S301 S304 |
| 174763 | BAA02g17520 | A02 | 8735285 | C | T | upstream_gene_variant | MODIFIER | c.-2470G>A| |
S208 S219 |
| 174764 | BAA02g17520 | A02 | 8735598 | G | A | upstream_gene_variant | MODIFIER | c.-2783C>T| |
S293 |
| 174765 | BAA02g17520 | A02 | 8735916 | G | A | upstream_gene_variant | MODIFIER | c.-3101C>T| |
S297 |
| 174766 | BAA02g17520 | A02 | 8736871 | C | T | upstream_gene_variant | MODIFIER | c.-4056G>A| |
S206 S26 |
| 174767 | BAA02g17530 | A02 | 8737383 | G | A | synonymous_variant | LOW | c.706C>T|p.Leu236Leu |
S139 |
| 174768 | BAA02g17530 | A02 | 8737955 | G | A | missense_variant | MODERATE | c.517C>T|p.Leu173Phe |
S238 |
| 174769 | BAA02g17530 | A02 | 8739139 | C | T | upstream_gene_variant | MODIFIER | c.-216G>A| |
S87 |
| 174770 | BAA02g17530 | A02 | 8739441 | C | T | upstream_gene_variant | MODIFIER | c.-518G>A| |
S159 S188 S243 S276 S298 S299 |
| 174771 | BAA02g17530 | A02 | 8740559 | G | A | upstream_gene_variant | MODIFIER | c.-1636C>T| |
S168 |
| 174772 | BAA02g17530 | A02 | 8740764 | C | T | upstream_gene_variant | MODIFIER | c.-1841G>A| |
S179 |
| 174773 | BAA02g17530 | A02 | 8741698 | C | T | upstream_gene_variant | MODIFIER | c.-2775G>A| |
S218 |
| 174774 | BAA02g17530 | A02 | 8742302 | G | A | upstream_gene_variant | MODIFIER | c.-3379C>T| |
S148 S30 S31 |
| 174775 | BAA02g17530 | A02 | 8742593 | G | A | upstream_gene_variant | MODIFIER | c.-3670C>T| |
S26 |