Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g13740 | A10 | 14723278 | C | T | missense_variant | MODERATE | c.257G>A|p.Gly86Asp |
S202 |
2 | BAA10g13740 | A10 | 14724248 | C | T | upstream_gene_variant | MODIFIER | c.-714G>A| |
S202 |
3 | BAA10g13740 | A10 | 14724704 | C | T | upstream_gene_variant | MODIFIER | c.-1170G>A| |
S275 |
4 | BAA10g13740 | A10 | 14725350 | C | T | upstream_gene_variant | MODIFIER | c.-1816G>A| |
S116 |
5 | BAA10g13740 | A10 | 14726123 | C | T | upstream_gene_variant | MODIFIER | c.-2589G>A| |
S238 |
6 | BAA10g13740 | A10 | 14726767 | G | A | upstream_gene_variant | MODIFIER | c.-3233C>T| |
S198 |
7 | BAA10g13740 | A10 | 14727571 | C | T | upstream_gene_variant | MODIFIER | c.-4037G>A| |
S44 |
8 | BAA10g13740 | A10 | 14727667 | C | T | upstream_gene_variant | MODIFIER | c.-4133G>A| |
S146 |