Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g06000 | A10 | 3075573 | G | A | upstream_gene_variant | MODIFIER | c.-3820G>A| |
S221 |
2 | BAA10g06000 | A10 | 3076800 | C | T | upstream_gene_variant | MODIFIER | c.-2593C>T| |
S256 |
3 | BAA10g06000 | A10 | 3077000 | C | T | upstream_gene_variant | MODIFIER | c.-2393C>T| |
S259 |
4 | BAA10g06000 | A10 | 3077230 | C | T | upstream_gene_variant | MODIFIER | c.-2163C>T| |
S169 |
5 | BAA10g06000 | A10 | 3077446 | C | T | upstream_gene_variant | MODIFIER | c.-1947C>T| |
S37 |
6 | BAA10g06000 | A10 | 3078814 | G | A | upstream_gene_variant | MODIFIER | c.-579G>A| |
S198 |
7 | BAA10g06000 | A10 | 3079342 | G | A | upstream_gene_variant | MODIFIER | c.-51G>A| |
S112 |
8 | BAA10g06000 | A10 | 3079547 | G | A | missense_variant | MODERATE | c.155G>A|p.Gly52Glu |
S262 |
9 | BAA10g06000 | A10 | 3081770 | C | T | missense_variant | MODERATE | c.1478C>T|p.Ala493Val |
S162 |
10 | BAA10g06000 | A10 | 3081886 | G | A | downstream_gene_variant | MODIFIER | c.*64G>A| |
S64 |
11 | BAA10g06000 | A10 | 3084028 | G | A | downstream_gene_variant | MODIFIER | c.*2206G>A| |
S111 |