Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g61860 | A09 | 58662042 | T | G | missense_variant | MODERATE | c.2336A>C|p.Asn779Thr |
S120 S13 S130 S131 S166 S208 S244 S269 S35 S43 S53 |
2 | BAA09g61860 | A09 | 58663025 | C | T | splice_region_variant&intron_variant | LOW | c.1946+3G>A| |
S171 |
3 | BAA09g61860 | A09 | 58663579 | C | T | synonymous_variant | LOW | c.1476G>A|p.Glu492Glu |
S208 |
4 | BAA09g61860 | A09 | 58664643 | C | T | synonymous_variant | LOW | c.579G>A|p.Arg193Arg |
S153 |
5 | BAA09g61860 | A09 | 58664895 | C | T | missense_variant | MODERATE | c.403G>A|p.Asp135Asn |
S26 |
6 | BAA09g61860 | A09 | 58665348 | C | T | missense_variant | MODERATE | c.28G>A|p.Val10Ile |
S124 |
7 | BAA09g61860 | A09 | 58665392 | C | T | upstream_gene_variant | MODIFIER | c.-17G>A| |
S295 |
8 | BAA09g61860 | A09 | 58665705 | G | A | upstream_gene_variant | MODIFIER | c.-330C>T| |
S54 |
9 | BAA09g61860 | A09 | 58665828 | C | T | upstream_gene_variant | MODIFIER | c.-453G>A| |
S226 |