Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g01390 | A05 | 803348 | G | A | missense_variant | MODERATE | c.2071C>T|p.Pro691Ser |
S7 |
2 | BAA05g01390 | A05 | 803894 | G | A | missense_variant | MODERATE | c.1676C>T|p.Pro559Leu |
S167 |
3 | BAA05g01390 | A05 | 804485 | C | T | stop_gained | HIGH | c.1245G>A|p.Trp415* |
S206 |
4 | BAA05g01390 | A05 | 805882 | C | T | missense_variant | MODERATE | c.316G>A|p.Asp106Asn |
S232 |
5 | BAA05g01390 | A05 | 806755 | G | A | upstream_gene_variant | MODIFIER | c.-469C>T| |
S158 |