Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g13060 | A09 | 7513132 | C | T | upstream_gene_variant | MODIFIER | c.-3860C>T| |
S30 S31 |
2 | BAA09g13060 | A09 | 7513525 | C | T | upstream_gene_variant | MODIFIER | c.-3467C>T| |
S71 |
3 | BAA09g13060 | A09 | 7515115 | C | T | upstream_gene_variant | MODIFIER | c.-1877C>T| |
S294 |
4 | BAA09g13060 | A09 | 7515419 | G | A | upstream_gene_variant | MODIFIER | c.-1573G>A| |
S259 |
5 | BAA09g13060 | A09 | 7516891 | C | T | upstream_gene_variant | MODIFIER | c.-101C>T| |
S153 |
6 | BAA09g13060 | A09 | 7517245 | C | T | synonymous_variant | LOW | c.120C>T|p.Asn40Asn |
S137 S215 |
7 | BAA09g13060 | A09 | 7518627 | C | T | missense_variant | MODERATE | c.776C>T|p.Ala259Val |
S217 S248 |
8 | BAA09g13060 | A09 | 7519451 | G | A | missense_variant&splice_region_variant | MODERATE | c.1297G>A|p.Ala433Thr |
S123 |
9 | BAA09g13060 | A09 | 7520192 | G | A | downstream_gene_variant | MODIFIER | c.*622G>A| |
S211 |
10 | BAA09g13060 | A09 | 7520659 | G | A | downstream_gene_variant | MODIFIER | c.*1089G>A| |
S16 |