Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g41150 | A02 | 34525270 | C | T | missense_variant | MODERATE | c.2432G>A|p.Gly811Glu |
S262 |
2 | BAA02g41150 | A02 | 34525456 | C | T | missense_variant | MODERATE | c.2246G>A|p.Arg749Lys |
S296 |
3 | BAA02g41150 | A02 | 34526970 | G | A | missense_variant | MODERATE | c.1171C>T|p.Pro391Ser |
S217 S80 |
4 | BAA02g41150 | A02 | 34527420 | G | A | missense_variant | MODERATE | c.880C>T|p.Pro294Ser |
S35 |
5 | BAA02g41150 | A02 | 34528533 | G | A | upstream_gene_variant | MODIFIER | c.-234C>T| |
S142 |
6 | BAA02g41150 | A02 | 34529071 | C | T | upstream_gene_variant | MODIFIER | c.-772G>A| |
S255 |
7 | BAA02g41150 | A02 | 34529826 | C | T | upstream_gene_variant | MODIFIER | c.-1527G>A| |
S218 |
8 | BAA02g41150 | A02 | 34530777 | C | T | upstream_gene_variant | MODIFIER | c.-2478G>A| |
S32 |
9 | BAA02g41150 | A02 | 34532080 | C | T | upstream_gene_variant | MODIFIER | c.-3781G>A| |
S87 |
10 | BAA02g41150 | A02 | 34532140 | C | T | upstream_gene_variant | MODIFIER | c.-3841G>A| |
S116 |
11 | BAA02g41150 | A02 | 34533157 | G | A | upstream_gene_variant | MODIFIER | c.-4858C>T| |
S302 |