Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g66570 | A09 | 60771886 | G | A | missense_variant | MODERATE | c.2813C>T|p.Pro938Leu |
S72 S78 |
2 | BAA09g66570 | A09 | 60772019 | C | T | missense_variant | MODERATE | c.2680G>A|p.Asp894Asn |
S257 |
3 | BAA09g66570 | A09 | 60773271 | C | T | missense_variant | MODERATE | c.1790G>A|p.Ser597Asn |
S6 |
4 | BAA09g66570 | A09 | 60773832 | C | T | missense_variant | MODERATE | c.1417G>A|p.Glu473Lys |
S186 |
5 | BAA09g66570 | A09 | 60774407 | C | T | missense_variant | MODERATE | c.938G>A|p.Arg313Lys |
S159 S299 |
6 | BAA09g66570 | A09 | 60775768 | G | A | upstream_gene_variant | MODIFIER | c.-424C>T| |
S247 |
7 | BAA09g66570 | A09 | 60776858 | C | T | upstream_gene_variant | MODIFIER | c.-1514G>A| |
S94 |
8 | BAA09g66570 | A09 | 60778569 | G | A | upstream_gene_variant | MODIFIER | c.-3225C>T| |
S286 |