Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g02150 | A01 | 987575 | G | A | upstream_gene_variant | MODIFIER | c.-4881G>A| |
S84 |
2 | BAA01g02150 | A01 | 987584 | C | A | upstream_gene_variant | MODIFIER | c.-4872C>A| |
|
3 | BAA01g02150 | A01 | 988704 | C | T | upstream_gene_variant | MODIFIER | c.-3752C>T| |
S208 S219 |
4 | BAA01g02150 | A01 | 988760 | G | A | upstream_gene_variant | MODIFIER | c.-3696G>A| |
S159 S243 |
5 | BAA01g02150 | A01 | 989853 | C | T | upstream_gene_variant | MODIFIER | c.-2603C>T| |
S179 |
6 | BAA01g02150 | A01 | 989979 | T | G | upstream_gene_variant | MODIFIER | c.-2477T>G| |
S113 |
7 | BAA01g02150 | A01 | 991751 | C | T | upstream_gene_variant | MODIFIER | c.-705C>T| |
S66 |
8 | BAA01g02150 | A01 | 991830 | G | A | upstream_gene_variant | MODIFIER | c.-626G>A| |
S12 |
9 | BAA01g02150 | A01 | 992555 | G | A | missense_variant | MODERATE | c.100G>A|p.Asp34Asn |
S67 |
10 | BAA01g02150 | A01 | 994047 | G | A | synonymous_variant | LOW | c.1026G>A|p.Glu342Glu |
S116 |