Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g18000 | A08 | 14510400 | C | T | missense_variant | MODERATE | c.64C>T|p.Leu22Phe |
S18 |
2 | BAA08g18000 | A08 | 14510964 | C | T | missense_variant | MODERATE | c.107C>T|p.Pro36Leu |
S183 S198 |
3 | BAA08g18000 | A08 | 14511429 | G | A | missense_variant | MODERATE | c.436G>A|p.Gly146Ser |
S297 |
4 | BAA08g18000 | A08 | 14514469 | G | A | downstream_gene_variant | MODIFIER | c.*2888G>A| |
S131 |
5 | BAA08g18000 | A08 | 14514485 | C | T | downstream_gene_variant | MODIFIER | c.*2904C>T| |
S67 |
6 | BAA08g18000 | A08 | 14516265 | C | T | downstream_gene_variant | MODIFIER | c.*4684C>T| |
S271 |