Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g01380 | A09 | 1013277 | G | A | downstream_gene_variant | MODIFIER | c.*4776C>T| |
S289 S290 |
2 | BAA09g01380 | A09 | 1013641 | G | A | downstream_gene_variant | MODIFIER | c.*4412C>T| |
S6 |
3 | BAA09g01380 | A09 | 1013706 | G | A | downstream_gene_variant | MODIFIER | c.*4347C>T| |
S293 |
4 | BAA09g01380 | A09 | 1013839 | C | T | downstream_gene_variant | MODIFIER | c.*4214G>A| |
S206 S26 |
5 | BAA09g01380 | A09 | 1017177 | C | T | downstream_gene_variant | MODIFIER | c.*876G>A| |
S71 |
6 | BAA09g01380 | A09 | 1018735 | C | T | missense_variant | MODERATE | c.3343G>A|p.Glu1115Lys |
S185 |
7 | BAA09g01380 | A09 | 1020031 | G | A | missense_variant | MODERATE | c.2381C>T|p.Thr794Ile |
S28 |
8 | BAA09g01380 | A09 | 1020112 | C | T | missense_variant | MODERATE | c.2300G>A|p.Gly767Glu |
S249 |
9 | BAA09g01380 | A09 | 1020579 | G | A | missense_variant | MODERATE | c.1991C>T|p.Ser664Phe |
S97 |
10 | BAA09g01380 | A09 | 1023838 | C | T | missense_variant | MODERATE | c.550G>A|p.Gly184Arg |
S64 |
11 | BAA09g01380 | A09 | 1024826 | G | A | upstream_gene_variant | MODIFIER | c.-174C>T| |
S123 |
12 | BAA09g01380 | A09 | 1026343 | G | A | upstream_gene_variant | MODIFIER | c.-1691C>T| |
S19 |