Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g01490 | A01 | 674944 | G | A | missense_variant | MODERATE | c.149C>T|p.Thr50Ile |
S188 |
2 | BAA01g01490 | A01 | 677556 | C | T | upstream_gene_variant | MODIFIER | c.-2045G>A| |
S278 |
3 | BAA01g01490 | A01 | 678746 | C | T | upstream_gene_variant | MODIFIER | c.-3235G>A| |
S171 |
4 | BAA01g01490 | A01 | 679803 | C | T | upstream_gene_variant | MODIFIER | c.-4292G>A| |
S100 |
5 | BAA01g01490 | A01 | 679863 | G | A | upstream_gene_variant | MODIFIER | c.-4352C>T| |
S221 |