Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g45390 | A02 | 37169306 | C | T | intron_variant | MODIFIER | c.264-43C>T| |
S58 |
2 | BAA02g45390 | A02 | 37169558 | C | T | missense_variant | MODERATE | c.473C>T|p.Ser158Phe |
S224 |
3 | BAA02g45390 | A02 | 37169978 | G | A | missense_variant | MODERATE | c.893G>A|p.Gly298Asp |
S37 |
4 | BAA02g45390 | A02 | 37171251 | G | A | downstream_gene_variant | MODIFIER | c.*1101G>A| |
S157 S163 |
5 | BAA02g45390 | A02 | 37172243 | C | T | downstream_gene_variant | MODIFIER | c.*2093C>T| |
S187 S250 |
6 | BAA02g45390 | A02 | 37172495 | C | T | downstream_gene_variant | MODIFIER | c.*2345C>T| |
S138 |
7 | BAA02g45390 | A02 | 37172559 | C | T | downstream_gene_variant | MODIFIER | c.*2409C>T| |
S130 |
8 | BAA02g45390 | A02 | 37174364 | G | A | downstream_gene_variant | MODIFIER | c.*4214G>A| |
S132 S137 S215 S89 |
9 | BAA02g45390 | A02 | 37174453 | C | T | downstream_gene_variant | MODIFIER | c.*4303C>T| |
S116 |