Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g05000 | A02 | 2177757 | G | T | upstream_gene_variant | MODIFIER | c.-3301G>T| |
S12 S138 S190 S201 S222 S25 S258 S264 S28 S282 S32 S70 |
2 | BAA02g05000 | A02 | 2178931 | G | A | upstream_gene_variant | MODIFIER | c.-2127G>A| |
S64 |
3 | BAA02g05000 | A02 | 2179143 | G | A | upstream_gene_variant | MODIFIER | c.-1915G>A| |
S34 |
4 | BAA02g05000 | A02 | 2179178 | G | A | upstream_gene_variant | MODIFIER | c.-1880G>A| |
S139 |
5 | BAA02g05000 | A02 | 2182540 | G | A | missense_variant | MODERATE | c.553G>A|p.Asp185Asn |
S198 |
6 | BAA02g05000 | A02 | 2182733 | C | T | missense_variant | MODERATE | c.746C>T|p.Ser249Phe |
S201 |
7 | BAA02g05000 | A02 | 2183111 | C | T | missense_variant | MODERATE | c.1022C>T|p.Ala341Val |
S174 |
8 | BAA02g05000 | A02 | 2183221 | G | A | missense_variant | MODERATE | c.1132G>A|p.Gly378Arg |
S153 S213 |
9 | BAA02g05000 | A02 | 2184681 | C | T | downstream_gene_variant | MODIFIER | c.*1236C>T| |
S144 |
10 | BAA02g05000 | A02 | 2185594 | G | A | downstream_gene_variant | MODIFIER | c.*2149G>A| |
S5 |