Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g00800 | A08 | 576303 | C | T | downstream_gene_variant | MODIFIER | c.*941G>A| |
S59 |
2 | BAA08g00800 | A08 | 576438 | G | A | downstream_gene_variant | MODIFIER | c.*806C>T| |
S16 |
3 | BAA08g00800 | A08 | 578597 | G | A | intron_variant | MODIFIER | c.1853+10C>T| |
S158 |
4 | BAA08g00800 | A08 | 579412 | C | T | intron_variant | MODIFIER | c.1510-123G>A| |
S133 |
5 | BAA08g00800 | A08 | 579645 | G | A | missense_variant | MODERATE | c.1468C>T|p.Arg490Cys |
S107 |
6 | BAA08g00800 | A08 | 579756 | C | T | missense_variant | MODERATE | c.1357G>A|p.Asp453Asn |
S36 |
7 | BAA08g00800 | A08 | 580051 | C | T | intron_variant | MODIFIER | c.1162-18G>A| |
S280 |
8 | BAA08g00800 | A08 | 580540 | C | T | synonymous_variant | LOW | c.918G>A|p.Thr306Thr |
S177 |
9 | BAA08g00800 | A08 | 580732 | C | T | intron_variant | MODIFIER | c.764-38G>A| |
S177 |
10 | BAA08g00800 | A08 | 582701 | C | T | upstream_gene_variant | MODIFIER | c.-784G>A| |
S38 |
11 | BAA08g00800 | A08 | 583497 | T | A | upstream_gene_variant | MODIFIER | c.-1580A>T| |
S260 |
12 | BAA08g00800 | A08 | 584134 | G | A | upstream_gene_variant | MODIFIER | c.-2217C>T| |
S112 |