Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g11390 | A07 | 20076210 | C | T | upstream_gene_variant | MODIFIER | c.-4659C>T| |
S132 S137 S215 |
2 | BAA07g11390 | A07 | 20077135 | C | T | upstream_gene_variant | MODIFIER | c.-3734C>T| |
S148 S30 |
3 | BAA07g11390 | A07 | 20078039 | C | T | upstream_gene_variant | MODIFIER | c.-2830C>T| |
S162 |
4 | BAA07g11390 | A07 | 20078562 | C | T | upstream_gene_variant | MODIFIER | c.-2307C>T| |
S79 S91 |
5 | BAA07g11390 | A07 | 20078581 | G | A | upstream_gene_variant | MODIFIER | c.-2288G>A| |
S115 |
6 | BAA07g11390 | A07 | 20079036 | C | T | upstream_gene_variant | MODIFIER | c.-1833C>T| |
S113 |
7 | BAA07g11390 | A07 | 20079823 | G | A | upstream_gene_variant | MODIFIER | c.-1046G>A| |
S288 |
8 | BAA07g11390 | A07 | 20081356 | C | T | intron_variant | MODIFIER | c.477+11C>T| |
S230 |
9 | BAA07g11390 | A07 | 20081769 | C | T | intron_variant | MODIFIER | c.552+256C>T| |
S155 |
10 | BAA07g11390 | A07 | 20082003 | C | T | intron_variant | MODIFIER | c.552+490C>T| |
S230 |
11 | BAA07g11390 | A07 | 20083191 | G | A | intron_variant | MODIFIER | c.759+165G>A| |
S95 |
12 | BAA07g11390 | A07 | 20083773 | G | A | intron_variant | MODIFIER | c.760-68G>A| |
S124 S51 |
13 | BAA07g11390 | A07 | 20084568 | G | A | downstream_gene_variant | MODIFIER | c.*452G>A| |
S206 S26 |
14 | BAA07g11390 | A07 | 20086037 | C | T | downstream_gene_variant | MODIFIER | c.*1921C>T| |
S303 |
15 | BAA07g11390 | A07 | 20087112 | C | T | downstream_gene_variant | MODIFIER | c.*2996C>T| |
S162 |
16 | BAA07g11390 | A07 | 20087572 | G | A | downstream_gene_variant | MODIFIER | c.*3456G>A| |
S71 |