Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g02890 | A06 | 1686058 | C | T | synonymous_variant | LOW | c.1350G>A|p.Val450Val |
S31 |
2 | BAA06g02890 | A06 | 1687035 | C | T | missense_variant | MODERATE | c.373G>A|p.Asp125Asn |
S293 |
3 | BAA06g02890 | A06 | 1688556 | G | A | upstream_gene_variant | MODIFIER | c.-1149C>T| |
S62 |
4 | BAA06g02890 | A06 | 1689169 | C | T | upstream_gene_variant | MODIFIER | c.-1762G>A| |
S116 |
5 | BAA06g02890 | A06 | 1689694 | G | A | upstream_gene_variant | MODIFIER | c.-2287C>T| |
S90 |
6 | BAA06g02890 | A06 | 1689853 | G | A | upstream_gene_variant | MODIFIER | c.-2446C>T| |
S294 |
7 | BAA06g02890 | A06 | 1690054 | G | A | upstream_gene_variant | MODIFIER | c.-2647C>T| |
S165 |
8 | BAA06g02890 | A06 | 1690487 | G | A | upstream_gene_variant | MODIFIER | c.-3080C>T| |
S128 |
9 | BAA06g02890 | A06 | 1691593 | C | T | upstream_gene_variant | MODIFIER | c.-4186G>A| |
S130 |