Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g01770 | A08 | 1304897 | G | A | downstream_gene_variant | MODIFIER | c.*2304C>T| |
S165 |
2 | BAA08g01770 | A08 | 1308220 | G | A | missense_variant | MODERATE | c.1177C>T|p.Leu393Phe |
S279 |
3 | BAA08g01770 | A08 | 1308987 | G | A | missense_variant | MODERATE | c.796C>T|p.Arg266Trp |
S37 |
4 | BAA08g01770 | A08 | 1309962 | C | T | upstream_gene_variant | MODIFIER | c.-99G>A| |
S126 |
5 | BAA08g01770 | A08 | 1310986 | G | A | upstream_gene_variant | MODIFIER | c.-1123C>T| |
S58 |
6 | BAA08g01770 | A08 | 1312983 | G | A | upstream_gene_variant | MODIFIER | c.-3120C>T| |
S306 S308 |
7 | BAA08g01770 | A08 | 1313288 | C | T | upstream_gene_variant | MODIFIER | c.-3425G>A| |
S132 S137 |
8 | BAA08g01770 | A08 | 1313557 | G | A | upstream_gene_variant | MODIFIER | c.-3694C>T| |
S16 |