Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g02280 | A01 | 1052840 | C | T | missense_variant | MODERATE | c.227G>A|p.Gly76Asp |
S168 |
2 | BAA01g02280 | A01 | 1055947 | G | A | upstream_gene_variant | MODIFIER | c.-2409C>T| |
S159 S243 |
3 | BAA01g02280 | A01 | 1056368 | G | A | upstream_gene_variant | MODIFIER | c.-2830C>T| |
S228 |
4 | BAA01g02280 | A01 | 1056541 | G | A | upstream_gene_variant | MODIFIER | c.-3003C>T| |
S190 |
5 | BAA01g02280 | A01 | 1057113 | C | T | upstream_gene_variant | MODIFIER | c.-3575G>A| |
S42 |
6 | BAA01g02280 | A01 | 1057223 | C | T | upstream_gene_variant | MODIFIER | c.-3685G>A| |
S48 |