Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g42050 | A02 | 35066039 | C | T | upstream_gene_variant | MODIFIER | c.-2777C>T| |
S187 |
2 | BAA02g42050 | A02 | 35066243 | C | T | upstream_gene_variant | MODIFIER | c.-2573C>T| |
S100 |
3 | BAA02g42050 | A02 | 35066680 | G | A | upstream_gene_variant | MODIFIER | c.-2136G>A| |
S164 |
4 | BAA02g42050 | A02 | 35066728 | C | T | upstream_gene_variant | MODIFIER | c.-2088C>T| |
S42 |
5 | BAA02g42050 | A02 | 35066846 | C | T | upstream_gene_variant | MODIFIER | c.-1970C>T| |
S295 |
6 | BAA02g42050 | A02 | 35069673 | G | A | missense_variant | MODERATE | c.365G>A|p.Arg122Gln |
S196 |
7 | BAA02g42050 | A02 | 35069973 | C | T | missense_variant | MODERATE | c.565C>T|p.Leu189Phe |
S104 S52 |
8 | BAA02g42050 | A02 | 35071138 | C | T | missense_variant | MODERATE | c.1256C>T|p.Ser419Phe |
S1 S90 |
9 | BAA02g42050 | A02 | 35072868 | G | A | downstream_gene_variant | MODIFIER | c.*1651G>A| |
S77 S82 |
10 | BAA02g42050 | A02 | 35073570 | C | T | downstream_gene_variant | MODIFIER | c.*2353C>T| |
S283 |
11 | BAA02g42050 | A02 | 35073771 | C | T | downstream_gene_variant | MODIFIER | c.*2554C>T| |
S277 |
12 | BAA02g42050 | A02 | 35074379 | C | T | downstream_gene_variant | MODIFIER | c.*3162C>T| |
S87 |
13 | BAA02g42050 | A02 | 35074975 | C | T | downstream_gene_variant | MODIFIER | c.*3758C>T| |
S203 |