Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g09950 | A01 | 4497647 | C | T | upstream_gene_variant | MODIFIER | c.-4684C>T| |
S128 |
2 | BAA01g09950 | A01 | 4497924 | C | T | upstream_gene_variant | MODIFIER | c.-4407C>T| |
S278 |
3 | BAA01g09950 | A01 | 4497946 | G | A | upstream_gene_variant | MODIFIER | c.-4385G>A| |
S186 |
4 | BAA01g09950 | A01 | 4498118 | G | A | upstream_gene_variant | MODIFIER | c.-4213G>A| |
S142 |
5 | BAA01g09950 | A01 | 4499210 | C | T | upstream_gene_variant | MODIFIER | c.-3121C>T| |
S144 |
6 | BAA01g09950 | A01 | 4499737 | G | A | upstream_gene_variant | MODIFIER | c.-2594G>A| |
S232 |
7 | BAA01g09950 | A01 | 4499820 | C | T | upstream_gene_variant | MODIFIER | c.-2511C>T| |
S77 |
8 | BAA01g09950 | A01 | 4500257 | G | A | upstream_gene_variant | MODIFIER | c.-2074G>A| |
S135 S185 S273 |
9 | BAA01g09950 | A01 | 4500491 | C | T | upstream_gene_variant | MODIFIER | c.-1840C>T| |
S185 |
10 | BAA01g09950 | A01 | 4501386 | C | T | upstream_gene_variant | MODIFIER | c.-945C>T| |
S18 |
11 | BAA01g09950 | A01 | 4501401 | G | A | upstream_gene_variant | MODIFIER | c.-930G>A| |
S92 |
12 | BAA01g09950 | A01 | 4501698 | G | A | upstream_gene_variant | MODIFIER | c.-633G>A| |
S297 |
13 | BAA01g09950 | A01 | 4502383 | C | T | missense_variant | MODERATE | c.53C>T|p.Thr18Ile |
S246 |