| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 176951 | BAA02g18610 | A02 | 9531809 | G | A | upstream_gene_variant | MODIFIER | c.-1119G>A| |
S153 S213 |
| 176952 | BAA02g18600 | A02 | 9532028 | C | T | missense_variant&splice_region_variant | MODERATE | c.26G>A|p.Ser9Asn |
S165 |
| 176953 | BAA02g18610 | A02 | 9535506 | G | A | missense_variant | MODERATE | c.1304G>A|p.Gly435Glu |
S193 |
| 176954 | BAA02g18600 | A02 | 9535799 | C | T | upstream_gene_variant | MODIFIER | c.-3746G>A| |
S255 |
| 176955 | BAA02g18600 | A02 | 9536827 | C | T | upstream_gene_variant | MODIFIER | c.-4774G>A| |
S55 |
| 176956 | BAA02g18610 | A02 | 9537081 | C | T | downstream_gene_variant | MODIFIER | c.*1544C>T| |
S2 |
| 176957 | BAA02g18610 | A02 | 9538893 | C | T | downstream_gene_variant | MODIFIER | c.*3356C>T| |
S261 |
| 176958 | BAA02g18610 | A02 | 9539607 | G | A | downstream_gene_variant | MODIFIER | c.*4070G>A| |
S281 |
| 176959 | BAA02g18620 | A02 | 9540501 | G | A | upstream_gene_variant | MODIFIER | c.-466C>T| |
S149 |
| 176960 | BAA02g18620 | A02 | 9540950 | C | T | upstream_gene_variant | MODIFIER | c.-915G>A| |
S123 |
| 176961 | BAA02g18620 | A02 | 9541129 | G | A | upstream_gene_variant | MODIFIER | c.-1094C>T| |
S237 |
| 176962 | BAA02g18620 | A02 | 9541265 | C | T | upstream_gene_variant | MODIFIER | c.-1230G>A| |
S174 |
| 176963 | BAA02g18620 | A02 | 9542188 | G | A | upstream_gene_variant | MODIFIER | c.-2153C>T| |
S23 |
| 176964 | BAA02g18620 | A02 | 9542233 | C | T | upstream_gene_variant | MODIFIER | c.-2198G>A| |
S221 |
| 176965 | BAA02g18630 | A02 | 9542425 | G | A | missense_variant | MODERATE | c.455C>T|p.Ala152Val |
S256 |
| 176966 | BAA02g18630 | A02 | 9542468 | C | T | missense_variant | MODERATE | c.412G>A|p.Val138Met |
S208 S219 |
| 176967 | BAA02g18630 | A02 | 9542524 | C | T | missense_variant | MODERATE | c.356G>A|p.Gly119Glu |
S75 S81 |
| 176968 | BAA02g18630 | A02 | 9542785 | C | T | stop_gained | HIGH | c.279G>A|p.Trp93* |
S277 |
| 176969 | BAA02g18620 | A02 | 9543278 | C | T | upstream_gene_variant | MODIFIER | c.-3243G>A| |
S268 |
| 176970 | BAA02g18620 | A02 | 9543927 | G | A | upstream_gene_variant | MODIFIER | c.-3892C>T| |
S111 |
| 176971 | BAA02g18620 | A02 | 9544097 | C | T | upstream_gene_variant | MODIFIER | c.-4062G>A| |
S142 |
| 176972 | BAA02g18620 | A02 | 9544762 | C | T | upstream_gene_variant | MODIFIER | c.-4727G>A| |
S267 |
| 176973 | BAA02g18620 | A02 | 9544792 | C | T | upstream_gene_variant | MODIFIER | c.-4757G>A| |
S80 |
| 176974 | BAA02g18640 | A02 | 9544898 | G | A | synonymous_variant | LOW | c.675C>T|p.Asn225Asn |
S125 |
| 176975 | BAA02g18630 | A02 | 9546759 | G | A | upstream_gene_variant | MODIFIER | c.-3602C>T| |
S166 |