Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g45910 | A09 | 50914768 | G | A | upstream_gene_variant | MODIFIER | c.-1214G>A| |
S143 |
2 | BAA09g45910 | A09 | 50915159 | G | A | upstream_gene_variant | MODIFIER | c.-823G>A| |
S289 S290 |
3 | BAA09g45910 | A09 | 50916046 | G | A | missense_variant | MODERATE | c.65G>A|p.Gly22Glu |
S173 |
4 | BAA09g45910 | A09 | 50916508 | C | T | missense_variant | MODERATE | c.236C>T|p.Thr79Ile |
S302 |
5 | BAA09g45910 | A09 | 50917640 | G | A | missense_variant | MODERATE | c.629G>A|p.Gly210Glu |
S67 |
6 | BAA09g45910 | A09 | 50919839 | G | A | downstream_gene_variant | MODIFIER | c.*601G>A| |
S262 |
7 | BAA09g45910 | A09 | 50919859 | C | T | downstream_gene_variant | MODIFIER | c.*621C>T| |
S219 |
8 | BAA09g45910 | A09 | 50919872 | G | A | downstream_gene_variant | MODIFIER | c.*634G>A| |
S79 S91 |
9 | BAA09g45910 | A09 | 50920698 | C | T | downstream_gene_variant | MODIFIER | c.*1460C>T| |
S68 |
10 | BAA09g45910 | A09 | 50921021 | C | T | downstream_gene_variant | MODIFIER | c.*1783C>T| |
S38 |
11 | BAA09g45910 | A09 | 50921192 | G | A | downstream_gene_variant | MODIFIER | c.*1954G>A| |
S107 |