Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g23900 | A10 | 19909036 | G | A | missense_variant | MODERATE | c.1103C>T|p.Ser368Phe |
S134 |
2 | BAA10g23900 | A10 | 19909077 | C | T | synonymous_variant | LOW | c.1062G>A|p.Gln354Gln |
S230 |
3 | BAA10g23900 | A10 | 19910517 | G | A | missense_variant | MODERATE | c.334C>T|p.Leu112Phe |
S264 |
4 | BAA10g23900 | A10 | 19913093 | C | T | upstream_gene_variant | MODIFIER | c.-2158G>A| |
S210 |
5 | BAA10g23900 | A10 | 19915784 | C | T | upstream_gene_variant | MODIFIER | c.-4849G>A| |
S121 |
6 | BAA10g23900 | A10 | 19915789 | G | A | upstream_gene_variant | MODIFIER | c.-4854C>T| |
S263 |