Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g08770 | A08 | 8015712 | G | A | missense_variant | MODERATE | c.706C>T|p.Arg236Cys |
S35 |
2 | BAA08g08770 | A08 | 8017155 | C | T | upstream_gene_variant | MODIFIER | c.-244G>A| |
S294 |
3 | BAA08g08770 | A08 | 8019007 | G | A | upstream_gene_variant | MODIFIER | c.-2096C>T| |
S181 |
4 | BAA08g08770 | A08 | 8019038 | C | T | upstream_gene_variant | MODIFIER | c.-2127G>A| |
S226 |
5 | BAA08g08770 | A08 | 8019087 | C | T | upstream_gene_variant | MODIFIER | c.-2176G>A| |
S157 S163 |
6 | BAA08g08770 | A08 | 8019901 | G | A | upstream_gene_variant | MODIFIER | c.-2990C>T| |
S158 |
7 | BAA08g08770 | A08 | 8020135 | G | A | upstream_gene_variant | MODIFIER | c.-3224C>T| |
S202 |
8 | BAA08g08770 | A08 | 8020357 | G | A | upstream_gene_variant | MODIFIER | c.-3446C>T| |
S289 S290 |
9 | BAA08g08770 | A08 | 8020448 | C | T | upstream_gene_variant | MODIFIER | c.-3537G>A| |
S296 |
10 | BAA08g08770 | A08 | 8021313 | C | T | upstream_gene_variant | MODIFIER | c.-4402G>A| |
S209 |
11 | BAA08g08770 | A08 | 8021883 | C | T | upstream_gene_variant | MODIFIER | c.-4972G>A| |
S176 |