Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g34550 | A02 | 29623041 | C | T | synonymous_variant | LOW | c.267C>T|p.Tyr89Tyr |
S203 |
2 | BAA02g34550 | A02 | 29623817 | C | T | missense_variant | MODERATE | c.596C>T|p.Pro199Leu |
S308 |
3 | BAA02g34550 | A02 | 29624518 | C | T | synonymous_variant | LOW | c.741C>T|p.Thr247Thr |
S263 |
4 | BAA02g34550 | A02 | 29625119 | C | T | downstream_gene_variant | MODIFIER | c.*400C>T| |
S162 |
5 | BAA02g34550 | A02 | 29625143 | G | A | downstream_gene_variant | MODIFIER | c.*424G>A| |
S245 |
6 | BAA02g34550 | A02 | 29625430 | C | T | downstream_gene_variant | MODIFIER | c.*711C>T| |
S48 |
7 | BAA02g34550 | A02 | 29625523 | G | A | downstream_gene_variant | MODIFIER | c.*804G>A| |
S265 |
8 | BAA02g34550 | A02 | 29625560 | C | T | downstream_gene_variant | MODIFIER | c.*841C>T| |
S76 |
9 | BAA02g34550 | A02 | 29625908 | C | T | downstream_gene_variant | MODIFIER | c.*1189C>T| |
S173 |
10 | BAA02g34550 | A02 | 29625915 | C | T | downstream_gene_variant | MODIFIER | c.*1196C>T| |
S185 S304 |
11 | BAA02g34550 | A02 | 29625921 | C | T | downstream_gene_variant | MODIFIER | c.*1202C>T| |
S271 |
12 | BAA02g34550 | A02 | 29626562 | C | T | downstream_gene_variant | MODIFIER | c.*1843C>T| |
S164 |
13 | BAA02g34550 | A02 | 29626609 | C | T | downstream_gene_variant | MODIFIER | c.*1890C>T| |
S33 |
14 | BAA02g34550 | A02 | 29626807 | G | A | downstream_gene_variant | MODIFIER | c.*2088G>A| |
S43 |
15 | BAA02g34550 | A02 | 29627204 | C | T | downstream_gene_variant | MODIFIER | c.*2485C>T| |
S32 |