Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g46050 | A09 | 50984848 | G | A | upstream_gene_variant | MODIFIER | c.-3710G>A| |
S15 S3 |
2 | BAA09g46050 | A09 | 50985281 | G | A | upstream_gene_variant | MODIFIER | c.-3277G>A| |
S210 |
3 | BAA09g46050 | A09 | 50986353 | G | A | upstream_gene_variant | MODIFIER | c.-2205G>A| |
S128 |
4 | BAA09g46050 | A09 | 50986520 | C | T | upstream_gene_variant | MODIFIER | c.-2038C>T| |
S68 |
5 | BAA09g46050 | A09 | 50986751 | C | T | upstream_gene_variant | MODIFIER | c.-1807C>T| |
S140 |
6 | BAA09g46050 | A09 | 50986768 | G | A | upstream_gene_variant | MODIFIER | c.-1790G>A| |
S134 |
7 | BAA09g46050 | A09 | 50986808 | T | A | upstream_gene_variant | MODIFIER | c.-1750T>A| |
S279 |
8 | BAA09g46050 | A09 | 50987799 | C | T | upstream_gene_variant | MODIFIER | c.-759C>T| |
S237 |
9 | BAA09g46050 | A09 | 50988627 | C | T | missense_variant | MODERATE | c.70C>T|p.Pro24Ser |
S146 |
10 | BAA09g46050 | A09 | 50988629 | G | A | synonymous_variant | LOW | c.72G>A|p.Pro24Pro |
S42 |
11 | BAA09g46050 | A09 | 50990294 | G | A | synonymous_variant | LOW | c.1059G>A|p.Gln353Gln |
S36 |
12 | BAA09g46050 | A09 | 50991482 | C | T | downstream_gene_variant | MODIFIER | c.*1092C>T| |
S219 S72 |
13 | BAA09g46050 | A09 | 50993006 | C | T | downstream_gene_variant | MODIFIER | c.*2616C>T| |
S224 |
14 | BAA09g46050 | A09 | 50993036 | C | T | downstream_gene_variant | MODIFIER | c.*2646C>T| |
S250 |
15 | BAA09g46050 | A09 | 50993358 | C | T | downstream_gene_variant | MODIFIER | c.*2968C>T| |
S114 |
16 | BAA09g46050 | A09 | 50993641 | C | T | downstream_gene_variant | MODIFIER | c.*3251C>T| |
S89 |
17 | BAA09g46050 | A09 | 50993771 | C | T | downstream_gene_variant | MODIFIER | c.*3381C>T| |
S80 |
18 | BAA09g46050 | A09 | 50995041 | G | A | downstream_gene_variant | MODIFIER | c.*4651G>A| |
S53 |