Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g03850 | A10 | 1874266 | G | A | missense_variant | MODERATE | c.539C>T|p.Thr180Ile |
S45 |
2 | BAA10g03850 | A10 | 1874389 | C | T | missense_variant | MODERATE | c.416G>A|p.Cys139Tyr |
S270 |
3 | BAA10g03850 | A10 | 1875064 | G | A | missense_variant | MODERATE | c.136C>T|p.Leu46Phe |
S221 |
4 | BAA10g03850 | A10 | 1878281 | C | T | upstream_gene_variant | MODIFIER | c.-3082G>A| |
S176 S191 |
5 | BAA10g03850 | A10 | 1879059 | C | T | upstream_gene_variant | MODIFIER | c.-3860G>A| |
S123 |