Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g19210 | A02 | 9974851 | G | A | missense_variant | MODERATE | c.196G>A|p.Ala66Thr |
S84 S93 |
2 | BAA02g19210 | A02 | 9975952 | C | T | missense_variant | MODERATE | c.790C>T|p.Leu264Phe |
S100 |
3 | BAA02g19210 | A02 | 9978105 | G | A | downstream_gene_variant | MODIFIER | c.*1127G>A| |
S126 |
4 | BAA02g19210 | A02 | 9978763 | G | A | downstream_gene_variant | MODIFIER | c.*1785G>A| |
S146 |
5 | BAA02g19210 | A02 | 9979124 | T | G | downstream_gene_variant | MODIFIER | c.*2146T>G| |
S140 |
6 | BAA02g19210 | A02 | 9979711 | G | A | downstream_gene_variant | MODIFIER | c.*2733G>A| |
S279 |
7 | BAA02g19210 | A02 | 9980294 | G | A | downstream_gene_variant | MODIFIER | c.*3316G>A| |
S132 S137 S215 |
8 | BAA02g19210 | A02 | 9980764 | G | A | downstream_gene_variant | MODIFIER | c.*3786G>A| |
S162 |
9 | BAA02g19210 | A02 | 9981752 | C | T | downstream_gene_variant | MODIFIER | c.*4774C>T| |
S163 |