Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g24960 | A09 | 16034293 | G | A | downstream_gene_variant | MODIFIER | c.*3117C>T| |
S112 |
2 | BAA09g24960 | A09 | 16034367 | C | T | downstream_gene_variant | MODIFIER | c.*3043G>A| |
S277 |
3 | BAA09g24960 | A09 | 16034715 | G | A | downstream_gene_variant | MODIFIER | c.*2695C>T| |
S1 S90 |
4 | BAA09g24960 | A09 | 16034835 | G | A | downstream_gene_variant | MODIFIER | c.*2575C>T| |
S295 |
5 | BAA09g24960 | A09 | 16034969 | G | A | downstream_gene_variant | MODIFIER | c.*2441C>T| |
S126 |
6 | BAA09g24960 | A09 | 16035025 | G | A | downstream_gene_variant | MODIFIER | c.*2385C>T| |
S210 S225 |
7 | BAA09g24960 | A09 | 16035530 | G | A | downstream_gene_variant | MODIFIER | c.*1880C>T| |
S201 |
8 | BAA09g24960 | A09 | 16036041 | C | T | downstream_gene_variant | MODIFIER | c.*1369G>A| |
S5 |
9 | BAA09g24960 | A09 | 16038912 | C | T | synonymous_variant | LOW | c.312G>A|p.Leu104Leu |
S289 S290 |
10 | BAA09g24960 | A09 | 16039253 | G | A | missense_variant | MODERATE | c.122C>T|p.Thr41Ile |
S284 |
11 | BAA09g24960 | A09 | 16041987 | G | A | upstream_gene_variant | MODIFIER | c.-2613C>T| |
S86 |
12 | BAA09g24960 | A09 | 16043596 | C | T | upstream_gene_variant | MODIFIER | c.-4222G>A| |
S268 |
13 | BAA09g24960 | A09 | 16043740 | G | A | upstream_gene_variant | MODIFIER | c.-4366C>T| |
S189 |
14 | BAA09g24960 | A09 | 16043763 | C | T | upstream_gene_variant | MODIFIER | c.-4389G>A| |
S159 S243 S299 |
15 | BAA09g24960 | A09 | 16044067 | G | A | upstream_gene_variant | MODIFIER | c.-4693C>T| |
S303 |
16 | BAA09g24960 | A09 | 16044147 | G | A | upstream_gene_variant | MODIFIER | c.-4773C>T| |
S197 |