Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g20460 | A02 | 10857465 | G | A | missense_variant | MODERATE | c.1294C>T|p.Arg432Cys |
S64 |
2 | BAA02g20460 | A02 | 10857516 | G | A | missense_variant | MODERATE | c.1243C>T|p.Pro415Ser |
S64 |
3 | BAA02g20460 | A02 | 10858530 | C | T | missense_variant | MODERATE | c.562G>A|p.Val188Met |
S244 |
4 | BAA02g20460 | A02 | 10861389 | G | A | upstream_gene_variant | MODIFIER | c.-1914C>T| |
S161 |
5 | BAA02g20460 | A02 | 10861405 | G | A | upstream_gene_variant | MODIFIER | c.-1930C>T| |
S303 |
6 | BAA02g20460 | A02 | 10861573 | G | A | upstream_gene_variant | MODIFIER | c.-2098C>T| |
S306 S308 |
7 | BAA02g20460 | A02 | 10861751 | G | A | upstream_gene_variant | MODIFIER | c.-2276C>T| |
S122 |
8 | BAA02g20460 | A02 | 10863378 | C | T | upstream_gene_variant | MODIFIER | c.-3903G>A| |
S99 |
9 | BAA02g20460 | A02 | 10863599 | G | A | upstream_gene_variant | MODIFIER | c.-4124C>T| |
S148 |
10 | BAA02g20460 | A02 | 10864125 | C | T | upstream_gene_variant | MODIFIER | c.-4650G>A| |
S270 |