Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g00900 | A01 | 395066 | C | T | missense_variant | MODERATE | c.640G>A|p.Gly214Arg |
S19 |
2 | BAA01g00900 | A01 | 396463 | G | A | upstream_gene_variant | MODIFIER | c.-145C>T| |
S142 |
3 | BAA01g00900 | A01 | 396823 | G | A | upstream_gene_variant | MODIFIER | c.-505C>T| |
S275 |
4 | BAA01g00900 | A01 | 400155 | G | A | upstream_gene_variant | MODIFIER | c.-3837C>T| |
S186 |