Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g12660 | A10 | 14058147 | C | T | downstream_gene_variant | MODIFIER | c.*2069G>A| |
S28 |
2 | BAA10g12660 | A10 | 14058504 | C | T | downstream_gene_variant | MODIFIER | c.*1712G>A| |
S42 |
3 | BAA10g12660 | A10 | 14061826 | G | A | synonymous_variant | LOW | c.228C>T|p.Phe76Phe |
S241 |
4 | BAA10g12660 | A10 | 14062825 | G | A | upstream_gene_variant | MODIFIER | c.-772C>T| |
S209 |
5 | BAA10g12660 | A10 | 14062846 | G | A | upstream_gene_variant | MODIFIER | c.-793C>T| |
S261 |
6 | BAA10g12660 | A10 | 14062956 | C | T | upstream_gene_variant | MODIFIER | c.-903G>A| |
S121 |
7 | BAA10g12660 | A10 | 14063088 | C | T | upstream_gene_variant | MODIFIER | c.-1035G>A| |
S25 |
8 | BAA10g12660 | A10 | 14063343 | G | A | upstream_gene_variant | MODIFIER | c.-1290C>T| |
S129 |
9 | BAA10g12660 | A10 | 14064134 | C | T | upstream_gene_variant | MODIFIER | c.-2081G>A| |
S140 |
10 | BAA10g12660 | A10 | 14066359 | G | A | upstream_gene_variant | MODIFIER | c.-4306C>T| |
S48 |
11 | BAA10g12660 | A10 | 14066400 | C | T | upstream_gene_variant | MODIFIER | c.-4347G>A| |
S149 |
12 | BAA10g12660 | A10 | 14066810 | C | T | upstream_gene_variant | MODIFIER | c.-4757G>A| |
S183 |