Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g00010 | A04 | 2770 | G | A | downstream_gene_variant | MODIFIER | c.*4870C>T| |
S120 |
2 | BAA04g00010 | A04 | 2788 | C | T | downstream_gene_variant | MODIFIER | c.*4852G>A| |
S206 S26 |
3 | BAA04g00010 | A04 | 3025 | G | A | downstream_gene_variant | MODIFIER | c.*4615C>T| |
S156 |
4 | BAA04g00010 | A04 | 3221 | G | A | downstream_gene_variant | MODIFIER | c.*4419C>T| |
S188 |
5 | BAA04g00010 | A04 | 3289 | G | A | downstream_gene_variant | MODIFIER | c.*4351C>T| |
S133 |
6 | BAA04g00010 | A04 | 3417 | G | A | downstream_gene_variant | MODIFIER | c.*4223C>T| |
S144 |
7 | BAA04g00010 | A04 | 3513 | C | T | downstream_gene_variant | MODIFIER | c.*4127G>A| |
S178 |
8 | BAA04g00010 | A04 | 5088 | G | A | downstream_gene_variant | MODIFIER | c.*2552C>T| |
S112 S67 |
9 | BAA04g00010 | A04 | 5639 | G | A | downstream_gene_variant | MODIFIER | c.*2001C>T| |
S126 |
10 | BAA04g00010 | A04 | 5652 | C | T | downstream_gene_variant | MODIFIER | c.*1988G>A| |
S257 |
11 | BAA04g00010 | A04 | 5660 | C | A | downstream_gene_variant | MODIFIER | c.*1980G>T| |
S109 |
12 | BAA04g00010 | A04 | 5851 | G | A | downstream_gene_variant | MODIFIER | c.*1789C>T| |
S12 S308 |
13 | BAA04g00010 | A04 | 8393 | C | T | upstream_gene_variant | MODIFIER | c.-292G>A| |
S129 |
14 | BAA04g00010 | A04 | 9910 | G | A | upstream_gene_variant | MODIFIER | c.-1809C>T| |
S303 |
15 | BAA04g00010 | A04 | 10393 | C | T | upstream_gene_variant | MODIFIER | c.-2292G>A| |
S301 S304 |
16 | BAA04g00010 | A04 | 11613 | C | T | upstream_gene_variant | MODIFIER | c.-3512G>A| |
S209 |