Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g21460 | A01 | 10641958 | G | A | upstream_gene_variant | MODIFIER | c.-3788G>A| |
S163 |
2 | BAA01g21460 | A01 | 10642456 | C | T | upstream_gene_variant | MODIFIER | c.-3290C>T| |
S203 |
3 | BAA01g21460 | A01 | 10642715 | G | A | upstream_gene_variant | MODIFIER | c.-3031G>A| |
S87 |
4 | BAA01g21460 | A01 | 10642762 | C | T | upstream_gene_variant | MODIFIER | c.-2984C>T| |
S128 S143 |
5 | BAA01g21460 | A01 | 10643294 | C | T | upstream_gene_variant | MODIFIER | c.-2452C>T| |
S221 |
6 | BAA01g21460 | A01 | 10644683 | G | A | upstream_gene_variant | MODIFIER | c.-1063G>A| |
S2 |
7 | BAA01g21460 | A01 | 10645033 | C | T | upstream_gene_variant | MODIFIER | c.-713C>T| |
S61 |
8 | BAA01g21460 | A01 | 10645536 | G | A | upstream_gene_variant | MODIFIER | c.-210G>A| |
S59 |
9 | BAA01g21460 | A01 | 10646687 | G | A | synonymous_variant | LOW | c.942G>A|p.Gln314Gln |
S159 S243 |
10 | BAA01g21460 | A01 | 10646958 | G | A | missense_variant | MODERATE | c.1213G>A|p.Asp405Asn |
S287 |
11 | BAA01g21460 | A01 | 10647087 | G | A | missense_variant | MODERATE | c.1342G>A|p.Asp448Asn |
S268 |