Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g19970 | A02 | 10482092 | G | A | missense_variant | MODERATE | c.1816C>T|p.Leu606Phe |
S136 |
2 | BAA02g19970 | A02 | 10484088 | C | T | missense_variant | MODERATE | c.574G>A|p.Glu192Lys |
S244 |
3 | BAA02g19970 | A02 | 10485362 | C | T | upstream_gene_variant | MODIFIER | c.-515G>A| |
S195 |
4 | BAA02g19970 | A02 | 10485424 | G | A | upstream_gene_variant | MODIFIER | c.-577C>T| |
S278 |
5 | BAA02g19970 | A02 | 10485518 | C | T | upstream_gene_variant | MODIFIER | c.-671G>A| |
S182 |
6 | BAA02g19970 | A02 | 10485533 | G | A | upstream_gene_variant | MODIFIER | c.-686C>T| |
S148 S30 S31 |
7 | BAA02g19970 | A02 | 10486945 | C | T | upstream_gene_variant | MODIFIER | c.-2098G>A| |
S80 |
8 | BAA02g19970 | A02 | 10487283 | C | T | upstream_gene_variant | MODIFIER | c.-2436G>A| |
S293 |
9 | BAA02g19970 | A02 | 10489002 | G | A | upstream_gene_variant | MODIFIER | c.-4155C>T| |
S190 |
10 | BAA02g19970 | A02 | 10489809 | C | T | upstream_gene_variant | MODIFIER | c.-4962G>A| |
S180 |