Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g19940 | A06 | 10434531 | C | T | missense_variant | MODERATE | c.590G>A|p.Gly197Glu |
S239 |
2 | BAA06g19940 | A06 | 10436000 | C | T | upstream_gene_variant | MODIFIER | c.-198G>A| |
S142 |
3 | BAA06g19940 | A06 | 10436024 | G | A | upstream_gene_variant | MODIFIER | c.-222C>T| |
S193 |
4 | BAA06g19940 | A06 | 10436603 | C | T | upstream_gene_variant | MODIFIER | c.-801G>A| |
S68 |
5 | BAA06g19940 | A06 | 10436747 | C | T | upstream_gene_variant | MODIFIER | c.-945G>A| |
S249 |
6 | BAA06g19940 | A06 | 10437515 | C | T | upstream_gene_variant | MODIFIER | c.-1713G>A| |
S112 |
7 | BAA06g19940 | A06 | 10438669 | G | A | upstream_gene_variant | MODIFIER | c.-2867C>T| |
S234 |
8 | BAA06g19940 | A06 | 10440065 | G | A | upstream_gene_variant | MODIFIER | c.-4263C>T| |
S39 |
9 | BAA06g19940 | A06 | 10440548 | C | T | upstream_gene_variant | MODIFIER | c.-4746G>A| |
S189 |