Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g10050 | A08 | 9155924 | T | C | upstream_gene_variant | MODIFIER | c.-874T>C| |
S111 |
2 | BAA08g10050 | A08 | 9156421 | C | T | upstream_gene_variant | MODIFIER | c.-377C>T| |
S152 |
3 | BAA08g10050 | A08 | 9157755 | C | T | missense_variant | MODERATE | c.265C>T|p.Leu89Phe |
S71 |
4 | BAA08g10050 | A08 | 9159029 | G | A | downstream_gene_variant | MODIFIER | c.*23G>A| |
S249 |
5 | BAA08g10050 | A08 | 9160475 | G | A | downstream_gene_variant | MODIFIER | c.*1469G>A| |
S265 |
6 | BAA08g10050 | A08 | 9161045 | G | A | downstream_gene_variant | MODIFIER | c.*2039G>A| |
S107 |
7 | BAA08g10050 | A08 | 9161767 | C | T | downstream_gene_variant | MODIFIER | c.*2761C>T| |
S36 |
8 | BAA08g10050 | A08 | 9162171 | G | A | downstream_gene_variant | MODIFIER | c.*3165G>A| |
S87 |
9 | BAA08g10050 | A08 | 9162882 | C | T | downstream_gene_variant | MODIFIER | c.*3876C>T| |
S201 |
10 | BAA08g10050 | A08 | 9162884 | G | A | downstream_gene_variant | MODIFIER | c.*3878G>A| |
S58 |
11 | BAA08g10050 | A08 | 9163129 | G | A | downstream_gene_variant | MODIFIER | c.*4123G>A| |
S20 |