Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g00700 | A05 | 398443 | C | T | downstream_gene_variant | MODIFIER | c.*2075G>A| |
S262 |
2 | BAA05g00700 | A05 | 399357 | G | A | downstream_gene_variant | MODIFIER | c.*1161C>T| |
S124 |
3 | BAA05g00700 | A05 | 400778 | G | A | missense_variant | MODERATE | c.574C>T|p.His192Tyr |
S296 |
4 | BAA05g00700 | A05 | 401266 | C | T | missense_variant | MODERATE | c.188G>A|p.Arg63Lys |
S197 |
5 | BAA05g00700 | A05 | 403052 | G | A | upstream_gene_variant | MODIFIER | c.-1510C>T| |
S134 |
6 | BAA05g00700 | A05 | 404153 | C | T | upstream_gene_variant | MODIFIER | c.-2611G>A| |
S96 |
7 | BAA05g00700 | A05 | 405116 | G | A | upstream_gene_variant | MODIFIER | c.-3574C>T| |
S294 |
8 | BAA05g00700 | A05 | 405329 | C | T | upstream_gene_variant | MODIFIER | c.-3787G>A| |
S15 S3 |