Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g26900 | A01 | 15177097 | G | A | downstream_gene_variant | MODIFIER | c.*769C>T| |
S45 |
2 | BAA01g26900 | A01 | 15178092 | G | A | synonymous_variant | LOW | c.1065C>T|p.Ile355Ile |
S181 |
3 | BAA01g26900 | A01 | 15178245 | G | A | intron_variant | MODIFIER | c.978-66C>T| |
S86 |
4 | BAA01g26900 | A01 | 15178413 | G | A | intron_variant | MODIFIER | c.978-234C>T| |
S60 |
5 | BAA01g26900 | A01 | 15178682 | G | A | intron_variant | MODIFIER | c.977+87C>T| |
S123 |
6 | BAA01g26900 | A01 | 15178737 | C | T | intron_variant | MODIFIER | c.977+32G>A| |
S208 |
7 | BAA01g26900 | A01 | 15178946 | C | T | missense_variant | MODERATE | c.800G>A|p.Arg267Lys |
S203 |
8 | BAA01g26900 | A01 | 15181442 | C | T | upstream_gene_variant | MODIFIER | c.-1697G>A| |
S18 |
9 | BAA01g26900 | A01 | 15183255 | C | T | upstream_gene_variant | MODIFIER | c.-3510G>A| |
S90 |
10 | BAA01g26900 | A01 | 15183412 | A | T | upstream_gene_variant | MODIFIER | c.-3667T>A| |
S236 |
11 | BAA01g26900 | A01 | 15184120 | C | T | upstream_gene_variant | MODIFIER | c.-4375G>A| |
S69 |