Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g34130 | A01 | 22811822 | C | T | missense_variant | MODERATE | c.127G>A|p.Asp43Asn |
S177 |
2 | BAA01g34130 | A01 | 22812386 | G | A | upstream_gene_variant | MODIFIER | c.-438C>T| |
S37 |
3 | BAA01g34130 | A01 | 22812538 | C | T | upstream_gene_variant | MODIFIER | c.-590G>A| |
S186 |
4 | BAA01g34130 | A01 | 22813398 | G | A | upstream_gene_variant | MODIFIER | c.-1450C>T| |
S187 |
5 | BAA01g34130 | A01 | 22813668 | C | T | upstream_gene_variant | MODIFIER | c.-1720G>A| |
S266 |
6 | BAA01g34130 | A01 | 22813947 | G | A | upstream_gene_variant | MODIFIER | c.-1999C>T| |
S218 |
7 | BAA01g34130 | A01 | 22814358 | G | A | upstream_gene_variant | MODIFIER | c.-2410C>T| |
S25 |
8 | BAA01g34130 | A01 | 22815174 | C | T | upstream_gene_variant | MODIFIER | c.-3226G>A| |
S28 |
9 | BAA01g34130 | A01 | 22815426 | G | A | upstream_gene_variant | MODIFIER | c.-3478C>T| |
S60 |
10 | BAA01g34130 | A01 | 22815786 | G | A | upstream_gene_variant | MODIFIER | c.-3838C>T| |
S175 |