Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g56600 | A03 | 28035965 | C | T | upstream_gene_variant | MODIFIER | c.-510C>T| |
S206 S26 |
2 | BAA03g56600 | A03 | 28035971 | C | T | upstream_gene_variant | MODIFIER | c.-504C>T| |
S163 |
3 | BAA03g56600 | A03 | 28036083 | G | A | upstream_gene_variant | MODIFIER | c.-392G>A| |
S246 |
4 | BAA03g56600 | A03 | 28036185 | C | T | upstream_gene_variant | MODIFIER | c.-290C>T| |
S155 |
5 | BAA03g56600 | A03 | 28036251 | C | T | upstream_gene_variant | MODIFIER | c.-224C>T| |
S89 |
6 | BAA03g56600 | A03 | 28037773 | C | T | missense_variant | MODERATE | c.941C>T|p.Ala314Val |
S8 |
7 | BAA03g56600 | A03 | 28038020 | C | T | synonymous_variant | LOW | c.1188C>T|p.Cys396Cys |
S116 |
8 | BAA03g56600 | A03 | 28038030 | G | A | missense_variant | MODERATE | c.1198G>A|p.Gly400Arg |
S294 |
9 | BAA03g56600 | A03 | 28038110 | C | T | synonymous_variant | LOW | c.1278C>T|p.Ile426Ile |
S183 S198 |
10 | BAA03g56600 | A03 | 28038153 | G | A | missense_variant | MODERATE | c.1321G>A|p.Glu441Lys |
S212 |
11 | BAA03g56600 | A03 | 28038406 | G | A | missense_variant | MODERATE | c.1574G>A|p.Gly525Glu |
S134 |
12 | BAA03g56600 | A03 | 28040361 | G | A | downstream_gene_variant | MODIFIER | c.*1099G>A| |
S20 |
13 | BAA03g56600 | A03 | 28040379 | C | T | downstream_gene_variant | MODIFIER | c.*1117C>T| |
S42 |
14 | BAA03g56600 | A03 | 28040865 | A | T | downstream_gene_variant | MODIFIER | c.*1603A>T| |
S161 |
15 | BAA03g56600 | A03 | 28040956 | C | T | downstream_gene_variant | MODIFIER | c.*1694C>T| |
S216 |
16 | BAA03g56600 | A03 | 28041235 | C | T | downstream_gene_variant | MODIFIER | c.*1973C>T| |
S298 |
17 | BAA03g56600 | A03 | 28041370 | G | A | downstream_gene_variant | MODIFIER | c.*2108G>A| |
S138 |
18 | BAA03g56600 | A03 | 28042698 | C | T | downstream_gene_variant | MODIFIER | c.*3436C>T| |
S179 |
19 | BAA03g56600 | A03 | 28043760 | C | T | downstream_gene_variant | MODIFIER | c.*4498C>T| |
S229 |