Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g18290 | A05 | 10476163 | C | T | missense_variant | MODERATE | c.148G>A|p.Gly50Arg |
S88 |
2 | BAA05g18290 | A05 | 10476215 | G | A | synonymous_variant | LOW | c.96C>T|p.Leu32Leu |
S156 |
3 | BAA05g18290 | A05 | 10476640 | C | T | upstream_gene_variant | MODIFIER | c.-330G>A| |
S246 |
4 | BAA05g18290 | A05 | 10477146 | C | T | upstream_gene_variant | MODIFIER | c.-836G>A| |
S63 |
5 | BAA05g18290 | A05 | 10477473 | G | A | upstream_gene_variant | MODIFIER | c.-1163C>T| |
S46 |
6 | BAA05g18290 | A05 | 10478124 | C | T | upstream_gene_variant | MODIFIER | c.-1814G>A| |
S209 |
7 | BAA05g18290 | A05 | 10478153 | G | A | upstream_gene_variant | MODIFIER | c.-1843C>T| |
S275 |
8 | BAA05g18290 | A05 | 10478795 | G | A | upstream_gene_variant | MODIFIER | c.-2485C>T| |
S244 |
9 | BAA05g18290 | A05 | 10478973 | C | T | upstream_gene_variant | MODIFIER | c.-2663G>A| |
S171 |
10 | BAA05g18290 | A05 | 10479204 | C | T | upstream_gene_variant | MODIFIER | c.-2894G>A| |
S45 |