Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g27460 | A01 | 15853857 | G | A | missense_variant | MODERATE | c.1499C>T|p.Ser500Phe |
S252 |
2 | BAA01g27460 | A01 | 15854019 | G | A | missense_variant | MODERATE | c.1337C>T|p.Thr446Ile |
S124 |
3 | BAA01g27460 | A01 | 15854110 | C | T | missense_variant | MODERATE | c.1246G>A|p.Gly416Arg |
S259 |
4 | BAA01g27460 | A01 | 15854571 | C | T | missense_variant | MODERATE | c.785G>A|p.Arg262Lys |
S179 |
5 | BAA01g27460 | A01 | 15854791 | C | T | missense_variant | MODERATE | c.565G>A|p.Glu189Lys |
S171 |
6 | BAA01g27460 | A01 | 15856659 | G | A | upstream_gene_variant | MODIFIER | c.-1304C>T| |
S86 |
7 | BAA01g27460 | A01 | 15856978 | G | A | upstream_gene_variant | MODIFIER | c.-1623C>T| |
S172 S217 |
8 | BAA01g27460 | A01 | 15856986 | C | T | upstream_gene_variant | MODIFIER | c.-1631G>A| |
S4 |
9 | BAA01g27460 | A01 | 15858555 | C | T | upstream_gene_variant | MODIFIER | c.-3200G>A| |
S171 |
10 | BAA01g27460 | A01 | 15858686 | G | A | upstream_gene_variant | MODIFIER | c.-3331C>T| |
S124 |