Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g30560 | A08 | 20614184 | G | A | missense_variant | MODERATE | c.1115C>T|p.Thr372Ile |
S46 |
2 | BAA08g30560 | A08 | 20614884 | G | A | missense_variant | MODERATE | c.503C>T|p.Pro168Leu |
S64 |
3 | BAA08g30560 | A08 | 20616283 | C | T | upstream_gene_variant | MODIFIER | c.-507G>A| |
S288 |
4 | BAA08g30560 | A08 | 20616525 | G | A | upstream_gene_variant | MODIFIER | c.-749C>T| |
S160 |
5 | BAA08g30560 | A08 | 20616841 | T | C | upstream_gene_variant | MODIFIER | c.-1065A>G| |
S218 |
6 | BAA08g30560 | A08 | 20617666 | C | T | upstream_gene_variant | MODIFIER | c.-1890G>A| |
S25 |
7 | BAA08g30560 | A08 | 20617713 | G | A | upstream_gene_variant | MODIFIER | c.-1937C>T| |
S296 |
8 | BAA08g30560 | A08 | 20617812 | C | T | upstream_gene_variant | MODIFIER | c.-2036G>A| |
S63 |
9 | BAA08g30560 | A08 | 20619142 | G | A | upstream_gene_variant | MODIFIER | c.-3366C>T| |
S221 |