Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g48640 | A09 | 52380556 | G | A | missense_variant | MODERATE | c.800C>T|p.Ala267Val |
S262 |
2 | BAA09g48640 | A09 | 52383115 | G | A | upstream_gene_variant | MODIFIER | c.-304C>T| |
S69 |
3 | BAA09g48640 | A09 | 52385056 | C | T | upstream_gene_variant | MODIFIER | c.-2245G>A| |
S63 |
4 | BAA09g48640 | A09 | 52385380 | C | T | upstream_gene_variant | MODIFIER | c.-2569G>A| |
S279 |
5 | BAA09g48640 | A09 | 52385443 | G | A | upstream_gene_variant | MODIFIER | c.-2632C>T| |
S233 |
6 | BAA09g48640 | A09 | 52386220 | C | T | upstream_gene_variant | MODIFIER | c.-3409G>A| |
S96 |
7 | BAA09g48640 | A09 | 52386289 | G | A | upstream_gene_variant | MODIFIER | c.-3478C>T| |
S48 |
8 | BAA09g48640 | A09 | 52387731 | G | A | upstream_gene_variant | MODIFIER | c.-4920C>T| |
S67 |