Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g00090 | A10 | 25561 | C | T | missense_variant | MODERATE | c.947G>A|p.Cys316Tyr |
S165 |
2 | BAA10g00090 | A10 | 25724 | C | T | missense_variant | MODERATE | c.868G>A|p.Glu290Lys |
S88 |
3 | BAA10g00090 | A10 | 29812 | G | A | upstream_gene_variant | MODIFIER | c.-3115C>T| |
S186 |
4 | BAA10g00090 | A10 | 29995 | C | T | upstream_gene_variant | MODIFIER | c.-3298G>A| |
S273 |
5 | BAA10g00090 | A10 | 30369 | C | T | upstream_gene_variant | MODIFIER | c.-3672G>A| |
S67 |
6 | BAA10g00090 | A10 | 31103 | C | T | upstream_gene_variant | MODIFIER | c.-4406G>A| |
S294 |
7 | BAA10g00090 | A10 | 31159 | G | A | upstream_gene_variant | MODIFIER | c.-4462C>T| |
S255 |
8 | BAA10g00090 | A10 | 31540 | G | A | upstream_gene_variant | MODIFIER | c.-4843C>T| |
S219 S72 |
9 | BAA10g00090 | A10 | 31621 | G | A | upstream_gene_variant | MODIFIER | c.-4924C>T| |
S138 |