Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g37690 | A03 | 17427068 | G | A | missense_variant | MODERATE | c.148G>A|p.Asp50Asn |
S89 |
2 | BAA03g37690 | A03 | 17427328 | C | T | synonymous_variant | LOW | c.330C>T|p.Val110Val |
S87 |
3 | BAA03g37690 | A03 | 17428168 | G | A | missense_variant | MODERATE | c.836G>A|p.Arg279Lys |
S289 S290 |
4 | BAA03g37690 | A03 | 17428355 | G | A | synonymous_variant | LOW | c.1023G>A|p.Ala341Ala |
S143 |
5 | BAA03g37690 | A03 | 17429335 | C | T | synonymous_variant | LOW | c.1506C>T|p.Phe502Phe |
S191 |
6 | BAA03g37690 | A03 | 17433439 | C | T | downstream_gene_variant | MODIFIER | c.*3523C>T| |
S105 S106 |
7 | BAA03g37690 | A03 | 17433709 | C | T | downstream_gene_variant | MODIFIER | c.*3793C>T| |
S142 |
8 | BAA03g37690 | A03 | 17434319 | G | A | downstream_gene_variant | MODIFIER | c.*4403G>A| |
S128 |
9 | BAA03g37690 | A03 | 17434356 | C | T | downstream_gene_variant | MODIFIER | c.*4440C>T| |
S89 |