Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g34250 | A01 | 22943293 | G | A | upstream_gene_variant | MODIFIER | c.-4307G>A| |
S121 |
2 | BAA01g34250 | A01 | 22946070 | C | T | upstream_gene_variant | MODIFIER | c.-1530C>T| |
S130 |
3 | BAA01g34250 | A01 | 22946322 | G | A | upstream_gene_variant | MODIFIER | c.-1278G>A| |
S114 |
4 | BAA01g34250 | A01 | 22946631 | G | A | upstream_gene_variant | MODIFIER | c.-969G>A| |
S208 |
5 | BAA01g34250 | A01 | 22946744 | C | T | upstream_gene_variant | MODIFIER | c.-856C>T| |
S275 |
6 | BAA01g34250 | A01 | 22948114 | G | A | intron_variant | MODIFIER | c.258+68G>A| |
S292 |
7 | BAA01g34250 | A01 | 22948731 | C | T | intron_variant | MODIFIER | c.390-14C>T| |
S261 |
8 | BAA01g34250 | A01 | 22948977 | G | A | intron_variant | MODIFIER | c.526-33G>A| |
S152 |
9 | BAA01g34250 | A01 | 22948994 | G | A | intron_variant | MODIFIER | c.526-16G>A| |
S163 |
10 | BAA01g34250 | A01 | 22949104 | G | A | missense_variant | MODERATE | c.620G>A|p.Ser207Asn |
S135 |
11 | BAA01g34250 | A01 | 22949290 | G | A | downstream_gene_variant | MODIFIER | c.*1G>A| |
S209 |
12 | BAA01g34250 | A01 | 22950387 | C | A | downstream_gene_variant | MODIFIER | c.*1098C>A| |
S223 |
13 | BAA01g34250 | A01 | 22950589 | C | T | downstream_gene_variant | MODIFIER | c.*1300C>T| |
S28 |