Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g24050 | A05 | 28997330 | C | T | upstream_gene_variant | MODIFIER | c.-4526C>T| |
S115 |
2 | BAA05g24050 | A05 | 28997650 | C | T | upstream_gene_variant | MODIFIER | c.-4206C>T| |
S35 |
3 | BAA05g24050 | A05 | 28998356 | G | A | upstream_gene_variant | MODIFIER | c.-3500G>A| |
S76 |
4 | BAA05g24050 | A05 | 28999246 | C | T | upstream_gene_variant | MODIFIER | c.-2610C>T| |
S274 |
5 | BAA05g24050 | A05 | 28999374 | G | A | upstream_gene_variant | MODIFIER | c.-2482G>A| |
S97 |
6 | BAA05g24050 | A05 | 28999629 | G | A | upstream_gene_variant | MODIFIER | c.-2227G>A| |
S249 |
7 | BAA05g24050 | A05 | 28999782 | G | A | upstream_gene_variant | MODIFIER | c.-2074G>A| |
S152 |
8 | BAA05g24050 | A05 | 29000099 | C | T | upstream_gene_variant | MODIFIER | c.-1757C>T| |
S268 |
9 | BAA05g24050 | A05 | 29000862 | G | A | upstream_gene_variant | MODIFIER | c.-994G>A| |
S257 |
10 | BAA05g24050 | A05 | 29001888 | C | T | synonymous_variant | LOW | c.33C>T|p.Arg11Arg |
S92 |
11 | BAA05g24050 | A05 | 29002064 | C | T | missense_variant | MODERATE | c.209C>T|p.Ser70Phe |
S287 |
12 | BAA05g24050 | A05 | 29003203 | G | A | missense_variant | MODERATE | c.854G>A|p.Cys285Tyr |
S244 |
13 | BAA05g24050 | A05 | 29004929 | G | A | downstream_gene_variant | MODIFIER | c.*1626G>A| |
S176 |
14 | BAA05g24050 | A05 | 29007068 | G | A | downstream_gene_variant | MODIFIER | c.*3765G>A| |
S166 S236 S257 |
15 | BAA05g24050 | A05 | 29007183 | C | T | downstream_gene_variant | MODIFIER | c.*3880C>T| |
S13 S168 S219 S64 S72 |
16 | BAA05g24050 | A05 | 29007428 | C | T | downstream_gene_variant | MODIFIER | c.*4125C>T| |
S17 |
17 | BAA05g24050 | A05 | 29007431 | C | T | downstream_gene_variant | MODIFIER | c.*4128C>T| |
S71 |
18 | BAA05g24050 | A05 | 29007565 | G | A | downstream_gene_variant | MODIFIER | c.*4262G>A| |
S192 |
19 | BAA05g24050 | A05 | 29008040 | G | A | downstream_gene_variant | MODIFIER | c.*4737G>A| |
S66 |