Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g26210 | A01 | 14548073 | G | A | upstream_gene_variant | MODIFIER | c.-4829G>A| |
S33 |
2 | BAA01g26210 | A01 | 14548958 | G | A | upstream_gene_variant | MODIFIER | c.-3944G>A| |
S252 |
3 | BAA01g26210 | A01 | 14549302 | G | A | upstream_gene_variant | MODIFIER | c.-3600G>A| |
S108 |
4 | BAA01g26210 | A01 | 14549474 | G | A | upstream_gene_variant | MODIFIER | c.-3428G>A| |
S57 |
5 | BAA01g26210 | A01 | 14549749 | C | T | upstream_gene_variant | MODIFIER | c.-3153C>T| |
S286 |
6 | BAA01g26210 | A01 | 14550906 | C | T | upstream_gene_variant | MODIFIER | c.-1996C>T| |
S35 |
7 | BAA01g26210 | A01 | 14552610 | C | T | upstream_gene_variant | MODIFIER | c.-292C>T| |
S10 |
8 | BAA01g26210 | A01 | 14552870 | C | T | upstream_gene_variant | MODIFIER | c.-32C>T| |
S155 S211 |
9 | BAA01g26210 | A01 | 14553266 | G | A | intron_variant | MODIFIER | c.229-31G>A| |
S280 |
10 | BAA01g26210 | A01 | 14553302 | G | A | synonymous_variant | LOW | c.234G>A|p.Leu78Leu |
S240 |
11 | BAA01g26210 | A01 | 14553464 | G | A | missense_variant | MODERATE | c.316G>A|p.Ala106Thr |
S149 |
12 | BAA01g26210 | A01 | 14553605 | G | A | intron_variant | MODIFIER | c.377+80G>A| |
S58 |
13 | BAA01g26210 | A01 | 14554652 | G | A | downstream_gene_variant | MODIFIER | c.*201G>A| |
S79 S91 |