Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g15950 | A10 | 16064213 | G | A | missense_variant | MODERATE | c.967C>T|p.Arg323Trp |
S103 |
2 | BAA10g15950 | A10 | 16064219 | C | T | missense_variant | MODERATE | c.961G>A|p.Asp321Asn |
S191 |
3 | BAA10g15950 | A10 | 16064541 | C | T | missense_variant | MODERATE | c.761G>A|p.Arg254Lys |
S256 |
4 | BAA10g15950 | A10 | 16064896 | G | T | splice_region_variant&intron_variant | LOW | c.615+8C>A| |
S308 |
5 | BAA10g15950 | A10 | 16066273 | C | T | missense_variant | MODERATE | c.142G>A|p.Glu48Lys |
S116 |
6 | BAA10g15950 | A10 | 16069531 | G | A | upstream_gene_variant | MODIFIER | c.-2960C>T| |
S165 |
7 | BAA10g15950 | A10 | 16070572 | C | T | upstream_gene_variant | MODIFIER | c.-4001G>A| |
S26 |