Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g05980 | A10 | 3070344 | G | A | missense_variant | MODERATE | c.40C>T|p.Pro14Ser |
S72 |
2 | BAA10g05980 | A10 | 3071287 | G | A | upstream_gene_variant | MODIFIER | c.-904C>T| |
S237 |
3 | BAA10g05980 | A10 | 3071357 | G | A | upstream_gene_variant | MODIFIER | c.-974C>T| |
S15 |
4 | BAA10g05980 | A10 | 3071996 | G | A | upstream_gene_variant | MODIFIER | c.-1613C>T| |
S153 S213 |
5 | BAA10g05980 | A10 | 3072235 | G | A | upstream_gene_variant | MODIFIER | c.-1852C>T| |
S209 |
6 | BAA10g05980 | A10 | 3072672 | G | A | upstream_gene_variant | MODIFIER | c.-2289C>T| |
S158 |
7 | BAA10g05980 | A10 | 3072817 | C | T | upstream_gene_variant | MODIFIER | c.-2434G>A| |
S256 |
8 | BAA10g05980 | A10 | 3073363 | G | A | upstream_gene_variant | MODIFIER | c.-2980C>T| |
S39 |
9 | BAA10g05980 | A10 | 3075145 | C | T | upstream_gene_variant | MODIFIER | c.-4762G>A| |
S140 |