Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g35650 | A08 | 22617249 | C | T | upstream_gene_variant | MODIFIER | c.-3777C>T| |
S116 |
2 | BAA08g35650 | A08 | 22617500 | C | T | upstream_gene_variant | MODIFIER | c.-3526C>T| |
S244 |
3 | BAA08g35650 | A08 | 22618816 | G | A | upstream_gene_variant | MODIFIER | c.-2210G>A| |
S233 |
4 | BAA08g35650 | A08 | 22621223 | C | T | synonymous_variant | LOW | c.198C>T|p.Ile66Ile |
S17 |
5 | BAA08g35650 | A08 | 22622350 | C | T | missense_variant | MODERATE | c.1325C>T|p.Pro442Leu |
S261 |
6 | BAA08g35650 | A08 | 22622384 | C | T | synonymous_variant | LOW | c.1359C>T|p.Phe453Phe |
S130 |
7 | BAA08g35650 | A08 | 22622640 | G | A | missense_variant | MODERATE | c.1615G>A|p.Gly539Arg |
S162 |
8 | BAA08g35650 | A08 | 22622760 | G | A | missense_variant | MODERATE | c.1735G>A|p.Glu579Lys |
S269 |
9 | BAA08g35650 | A08 | 22622813 | G | A | synonymous_variant | LOW | c.1788G>A|p.Ser596Ser |
S79 S91 |
10 | BAA08g35650 | A08 | 22622964 | C | T | missense_variant | MODERATE | c.1939C>T|p.Pro647Ser |
S50 |