Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g00170 | A02 | 118240 | C | T | upstream_gene_variant | MODIFIER | c.-2868C>T| |
S37 |
2 | BAA02g00170 | A02 | 120155 | C | T | upstream_gene_variant | MODIFIER | c.-953C>T| |
S207 |
3 | BAA02g00170 | A02 | 120762 | G | A | upstream_gene_variant | MODIFIER | c.-346G>A| |
S256 |
4 | BAA02g00170 | A02 | 120949 | G | A | upstream_gene_variant | MODIFIER | c.-159G>A| |
S184 |
5 | BAA02g00170 | A02 | 121383 | G | A | synonymous_variant | LOW | c.276G>A|p.Gly92Gly |
S265 |
6 | BAA02g00170 | A02 | 121697 | C | T | missense_variant | MODERATE | c.590C>T|p.Ser197Phe |
S267 |
7 | BAA02g00170 | A02 | 121753 | G | A | missense_variant | MODERATE | c.646G>A|p.Asp216Asn |
S44 |
8 | BAA02g00170 | A02 | 122169 | C | T | synonymous_variant | LOW | c.1062C>T|p.Ile354Ile |
S116 |
9 | BAA02g00170 | A02 | 122262 | C | T | synonymous_variant | LOW | c.1155C>T|p.Thr385Thr |
S281 |
10 | BAA02g00170 | A02 | 122969 | G | A | missense_variant | MODERATE | c.1862G>A|p.Gly621Glu |
S136 |
11 | BAA02g00170 | A02 | 124499 | C | T | downstream_gene_variant | MODIFIER | c.*1292C>T| |
S228 |
12 | BAA02g00170 | A02 | 125165 | G | A | downstream_gene_variant | MODIFIER | c.*1958G>A| |
S95 |
13 | BAA02g00170 | A02 | 125255 | C | T | downstream_gene_variant | MODIFIER | c.*2048C>T| |
S234 |