Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g00580 | A10 | 287436 | C | T | upstream_gene_variant | MODIFIER | c.-199C>T| |
S162 |
2 | BAA10g00580 | A10 | 287764 | G | A | missense_variant | MODERATE | c.130G>A|p.Gly44Arg |
S234 |
3 | BAA10g00580 | A10 | 287783 | G | C | missense_variant | MODERATE | c.149G>C|p.Ser50Thr |
S109 |
4 | BAA10g00580 | A10 | 287840 | C | T | missense_variant | MODERATE | c.206C>T|p.Pro69Leu |
S43 |
5 | BAA10g00580 | A10 | 287982 | C | T | synonymous_variant | LOW | c.348C>T|p.Val116Val |
S67 |
6 | BAA10g00580 | A10 | 288701 | C | T | missense_variant | MODERATE | c.1067C>T|p.Thr356Ile |
S139 |