Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g21120 | A10 | 18691201 | G | A | missense_variant | MODERATE | c.1124C>T|p.Ser375Phe |
S17 |
2 | BAA10g21120 | A10 | 18691458 | G | A | missense_variant | MODERATE | c.959C>T|p.Ala320Val |
S149 |
3 | BAA10g21120 | A10 | 18692380 | G | A | synonymous_variant | LOW | c.411C>T|p.His137His |
S134 |
4 | BAA10g21120 | A10 | 18693539 | C | T | upstream_gene_variant | MODIFIER | c.-442G>A| |
S153 S213 |
5 | BAA10g21120 | A10 | 18694280 | C | T | upstream_gene_variant | MODIFIER | c.-1183G>A| |
S83 S88 |