Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g03980 | A10 | 1945642 | G | A | downstream_gene_variant | MODIFIER | c.*4335C>T| |
S120 |
2 | BAA10g03980 | A10 | 1946079 | C | T | downstream_gene_variant | MODIFIER | c.*3898G>A| |
S256 |
3 | BAA10g03980 | A10 | 1946108 | G | A | downstream_gene_variant | MODIFIER | c.*3869C>T| |
S276 |
4 | BAA10g03980 | A10 | 1947058 | G | A | downstream_gene_variant | MODIFIER | c.*2919C>T| |
S33 |
5 | BAA10g03980 | A10 | 1947188 | G | A | downstream_gene_variant | MODIFIER | c.*2789C>T| |
S251 |
6 | BAA10g03980 | A10 | 1949171 | C | T | downstream_gene_variant | MODIFIER | c.*806G>A| |
S142 |
7 | BAA10g03980 | A10 | 1950533 | C | T | missense_variant | MODERATE | c.305G>A|p.Arg102Lys |
S271 S33 |
8 | BAA10g03980 | A10 | 1950588 | C | T | missense_variant | MODERATE | c.250G>A|p.Glu84Lys |
S87 |
9 | BAA10g03980 | A10 | 1950786 | C | T | missense_variant | MODERATE | c.52G>A|p.Asp18Asn |
S287 |
10 | BAA10g03980 | A10 | 1955299 | C | T | upstream_gene_variant | MODIFIER | c.-4161G>A| |
S308 S79 |