Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g11440 | A01 | 5295905 | C | T | missense_variant | MODERATE | c.859G>A|p.Gly287Arg |
S61 |
2 | BAA01g11440 | A01 | 5296065 | G | A | missense_variant | MODERATE | c.784C>T|p.Leu262Phe |
S116 |
3 | BAA01g11440 | A01 | 5296082 | C | T | missense_variant | MODERATE | c.767G>A|p.Gly256Glu |
S170 |
4 | BAA01g11440 | A01 | 5297958 | C | T | synonymous_variant | LOW | c.462G>A|p.Lys154Lys |
S54 |
5 | BAA01g11440 | A01 | 5299432 | G | A | upstream_gene_variant | MODIFIER | c.-509C>T| |
S239 |
6 | BAA01g11440 | A01 | 5299793 | G | A | upstream_gene_variant | MODIFIER | c.-870C>T| |
S149 |
7 | BAA01g11440 | A01 | 5299955 | C | T | upstream_gene_variant | MODIFIER | c.-1032G>A| |
S155 S211 |
8 | BAA01g11440 | A01 | 5303736 | C | T | upstream_gene_variant | MODIFIER | c.-4813G>A| |
S151 |
9 | BAA01g11440 | A01 | 5303781 | G | A | upstream_gene_variant | MODIFIER | c.-4858C>T| |
S241 |
10 | BAA01g11440 | A01 | 5303797 | G | A | upstream_gene_variant | MODIFIER | c.-4874C>T| |
S228 |