Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g05800 | A01 | 2583843 | C | T | synonymous_variant | LOW | c.594C>T|p.Leu198Leu |
S68 |
2 | BAA01g05800 | A01 | 2584370 | G | A | missense_variant | MODERATE | c.893G>A|p.Arg298His |
S140 |
3 | BAA01g05800 | A01 | 2585069 | G | A | missense_variant&splice_region_variant | MODERATE | c.1246G>A|p.Val416Ile |
S161 |
4 | BAA01g05800 | A01 | 2586100 | G | A | missense_variant | MODERATE | c.1726G>A|p.Glu576Lys |
S293 |
5 | BAA01g05800 | A01 | 2586160 | G | A | missense_variant | MODERATE | c.1786G>A|p.Asp596Asn |
S202 |
6 | BAA01g05800 | A01 | 2586718 | G | A | downstream_gene_variant | MODIFIER | c.*202G>A| |
S149 |
7 | BAA01g05800 | A01 | 2586817 | G | A | downstream_gene_variant | MODIFIER | c.*301G>A| |
S293 |
8 | BAA01g05800 | A01 | 2587288 | C | T | downstream_gene_variant | MODIFIER | c.*772C>T| |
S212 |
9 | BAA01g05800 | A01 | 2587838 | G | A | downstream_gene_variant | MODIFIER | c.*1322G>A| |
S144 |
10 | BAA01g05800 | A01 | 2588066 | G | A | downstream_gene_variant | MODIFIER | c.*1550G>A| |
S295 |
11 | BAA01g05800 | A01 | 2589445 | C | T | downstream_gene_variant | MODIFIER | c.*2929C>T| |
S273 |
12 | BAA01g05800 | A01 | 2590708 | G | A | downstream_gene_variant | MODIFIER | c.*4192G>A| |
S303 |