Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g45850 | A01 | 30557684 | C | T | missense_variant | MODERATE | c.140G>A|p.Gly47Asp |
S162 |
2 | BAA01g45850 | A01 | 30559731 | C | T | upstream_gene_variant | MODIFIER | c.-1378G>A| |
S233 |
3 | BAA01g45850 | A01 | 30560091 | C | T | upstream_gene_variant | MODIFIER | c.-1738G>A| |
S177 |
4 | BAA01g45850 | A01 | 30560163 | G | A | upstream_gene_variant | MODIFIER | c.-1810C>T| |
S71 |
5 | BAA01g45850 | A01 | 30560225 | C | T | upstream_gene_variant | MODIFIER | c.-1872G>A| |
S19 |
6 | BAA01g45850 | A01 | 30560387 | C | T | upstream_gene_variant | MODIFIER | c.-2034G>A| |
S73 S91 |
7 | BAA01g45850 | A01 | 30561040 | G | A | upstream_gene_variant | MODIFIER | c.-2687C>T| |
S108 |
8 | BAA01g45850 | A01 | 30561721 | C | T | upstream_gene_variant | MODIFIER | c.-3368G>A| |
S156 |
9 | BAA01g45850 | A01 | 30563037 | C | T | upstream_gene_variant | MODIFIER | c.-4684G>A| |
S126 |