Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g13050 | A01 | 6181964 | C | T | missense_variant | MODERATE | c.569G>A|p.Gly190Glu |
S38 |
2 | BAA01g13050 | A01 | 6183199 | G | A | upstream_gene_variant | MODIFIER | c.-326C>T| |
S308 |
3 | BAA01g13050 | A01 | 6184499 | G | A | upstream_gene_variant | MODIFIER | c.-1626C>T| |
S63 |
4 | BAA01g13050 | A01 | 6186581 | G | A | upstream_gene_variant | MODIFIER | c.-3708C>T| |
S297 |
5 | BAA01g13050 | A01 | 6186932 | C | T | upstream_gene_variant | MODIFIER | c.-4059G>A| |
S142 |