Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g36400 | A01 | 24392208 | C | T | downstream_gene_variant | MODIFIER | c.*3201G>A| |
S174 S27 |
2 | BAA01g36400 | A01 | 24395611 | G | A | missense_variant | MODERATE | c.1577C>T|p.Ala526Val |
S123 |
3 | BAA01g36400 | A01 | 24395856 | G | A | synonymous_variant | LOW | c.1332C>T|p.Leu444Leu |
S168 |
4 | BAA01g36400 | A01 | 24396576 | C | T | synonymous_variant | LOW | c.834G>A|p.Glu278Glu |
S148 S210 S30 S31 |
5 | BAA01g36400 | A01 | 24396899 | C | T | synonymous_variant | LOW | c.588G>A|p.Arg196Arg |
S289 S290 |
6 | BAA01g36400 | A01 | 24398012 | G | A | synonymous_variant | LOW | c.81C>T|p.Phe27Phe |
S262 |
7 | BAA01g36400 | A01 | 24399513 | G | A | upstream_gene_variant | MODIFIER | c.-1421C>T| |
S172 S217 |
8 | BAA01g36400 | A01 | 24399531 | C | G | upstream_gene_variant | MODIFIER | c.-1439G>C| |
S132 S137 S215 |
9 | BAA01g36400 | A01 | 24399666 | C | T | upstream_gene_variant | MODIFIER | c.-1574G>A| |
S153 |
10 | BAA01g36400 | A01 | 24401490 | C | T | upstream_gene_variant | MODIFIER | c.-3398G>A| |
S89 |
11 | BAA01g36400 | A01 | 24401696 | G | A | upstream_gene_variant | MODIFIER | c.-3604C>T| |
S197 S281 |
12 | BAA01g36400 | A01 | 24401784 | C | T | upstream_gene_variant | MODIFIER | c.-3692G>A| |
S288 |