Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g44070 | A02 | 36386860 | G | A | missense_variant | MODERATE | c.178G>A|p.Ala60Thr |
S13 |
2 | BAA02g44070 | A02 | 36388767 | C | T | missense_variant | MODERATE | c.524C>T|p.Ser175Phe |
S252 |
3 | BAA02g44070 | A02 | 36388890 | G | A | missense_variant | MODERATE | c.587G>A|p.Gly196Asp |
S247 |
4 | BAA02g44070 | A02 | 36390385 | C | T | missense_variant | MODERATE | c.1394C>T|p.Thr465Ile |
S122 |
5 | BAA02g44070 | A02 | 36390541 | C | T | splice_region_variant&intron_variant | LOW | c.1542+8C>T| |
S76 |
6 | BAA02g44070 | A02 | 36391645 | G | T | downstream_gene_variant | MODIFIER | c.*925G>T| |
S275 |
7 | BAA02g44070 | A02 | 36392021 | C | T | downstream_gene_variant | MODIFIER | c.*1301C>T| |
S266 |