Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g09850 | A10 | 11705037 | C | T | missense_variant | MODERATE | c.217G>A|p.Gly73Arg |
S225 S73 |
2 | BAA10g09850 | A10 | 11705364 | G | A | upstream_gene_variant | MODIFIER | c.-111C>T| |
S226 |
3 | BAA10g09850 | A10 | 11706773 | C | T | upstream_gene_variant | MODIFIER | c.-1520G>A| |
S84 S93 |
4 | BAA10g09850 | A10 | 11706927 | G | A | upstream_gene_variant | MODIFIER | c.-1674C>T| |
S66 |
5 | BAA10g09850 | A10 | 11707225 | G | A | upstream_gene_variant | MODIFIER | c.-1972C>T| |
S250 |
6 | BAA10g09850 | A10 | 11707505 | G | A | upstream_gene_variant | MODIFIER | c.-2252C>T| |
S176 |
7 | BAA10g09850 | A10 | 11708260 | G | A | upstream_gene_variant | MODIFIER | c.-3007C>T| |
S1 S90 |
8 | BAA10g09850 | A10 | 11708286 | C | T | upstream_gene_variant | MODIFIER | c.-3033G>A| |
S17 |
9 | BAA10g09850 | A10 | 11708432 | C | T | upstream_gene_variant | MODIFIER | c.-3179G>A| |
S131 |
10 | BAA10g09850 | A10 | 11709299 | C | T | upstream_gene_variant | MODIFIER | c.-4046G>A| |
S272 |