Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g15080 | A09 | 8615414 | C | T | missense_variant | MODERATE | c.527G>A|p.Arg176Lys |
S50 |
2 | BAA09g15080 | A09 | 8615652 | C | T | missense_variant | MODERATE | c.289G>A|p.Ala97Thr |
S39 |
3 | BAA09g15080 | A09 | 8615697 | G | A | missense_variant | MODERATE | c.244C>T|p.Pro82Ser |
S174 S241 S27 S39 |
4 | BAA09g15080 | A09 | 8618762 | G | A | upstream_gene_variant | MODIFIER | c.-2822C>T| |
S280 |
5 | BAA09g15080 | A09 | 8618949 | C | T | upstream_gene_variant | MODIFIER | c.-3009G>A| |
S294 |
6 | BAA09g15080 | A09 | 8619208 | G | A | upstream_gene_variant | MODIFIER | c.-3268C>T| |
S126 |
7 | BAA09g15080 | A09 | 8619259 | G | A | upstream_gene_variant | MODIFIER | c.-3319C>T| |
S45 |
8 | BAA09g15080 | A09 | 8619366 | G | A | upstream_gene_variant | MODIFIER | c.-3426C>T| |
S34 |
9 | BAA09g15080 | A09 | 8620732 | G | A | upstream_gene_variant | MODIFIER | c.-4792C>T| |
S288 |