Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g05060 | A02 | 2219988 | C | T | missense_variant | MODERATE | c.1126G>A|p.Ala376Thr |
S263 |
2 | BAA02g05060 | A02 | 2220690 | G | A | missense_variant | MODERATE | c.424C>T|p.Leu142Phe |
S263 |
3 | BAA02g05060 | A02 | 2220712 | C | A | missense_variant | MODERATE | c.402G>T|p.Leu134Phe |
S298 |
4 | BAA02g05060 | A02 | 2221511 | C | T | upstream_gene_variant | MODIFIER | c.-398G>A| |
S242 |
5 | BAA02g05060 | A02 | 2223278 | C | T | upstream_gene_variant | MODIFIER | c.-2165G>A| |
S71 |
6 | BAA02g05060 | A02 | 2223658 | C | T | upstream_gene_variant | MODIFIER | c.-2545G>A| |
S181 |
7 | BAA02g05060 | A02 | 2223807 | G | A | upstream_gene_variant | MODIFIER | c.-2694C>T| |
S259 |
8 | BAA02g05060 | A02 | 2225284 | C | T | upstream_gene_variant | MODIFIER | c.-4171G>A| |
S195 |
9 | BAA02g05060 | A02 | 2225995 | C | T | upstream_gene_variant | MODIFIER | c.-4882G>A| |
S16 |