Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g03750 | A10 | 1801407 | C | T | downstream_gene_variant | MODIFIER | c.*1246G>A| |
S197 |
2 | BAA10g03750 | A10 | 1802813 | G | A | missense_variant | MODERATE | c.1061C>T|p.Pro354Leu |
S216 |
3 | BAA10g03750 | A10 | 1804376 | G | A | missense_variant | MODERATE | c.205C>T|p.Arg69Cys |
S20 |
4 | BAA10g03750 | A10 | 1804400 | G | A | missense_variant | MODERATE | c.181C>T|p.Leu61Phe |
S18 |
5 | BAA10g03750 | A10 | 1807757 | C | T | upstream_gene_variant | MODIFIER | c.-3007G>A| |
S74 |
6 | BAA10g03750 | A10 | 1807995 | C | T | upstream_gene_variant | MODIFIER | c.-3245G>A| |
S210 S225 |
7 | BAA10g03750 | A10 | 1808148 | C | A | upstream_gene_variant | MODIFIER | c.-3398G>T| |
S1 S133 S143 S206 S238 S259 S267 S42 S58 S61 S92 S96 |
8 | BAA10g03750 | A10 | 1808861 | C | T | upstream_gene_variant | MODIFIER | c.-4111G>A| |
S297 |
9 | BAA10g03750 | A10 | 1808888 | C | T | upstream_gene_variant | MODIFIER | c.-4138G>A| |
S238 |
10 | BAA10g03750 | A10 | 1809750 | C | T | upstream_gene_variant | MODIFIER | c.-5000G>A| |
S142 |