Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g46200 | A09 | 51061037 | C | T | upstream_gene_variant | MODIFIER | c.-2581C>T| |
S75 |
2 | BAA09g46200 | A09 | 51061823 | C | T | upstream_gene_variant | MODIFIER | c.-1795C>T| |
S296 |
3 | BAA09g46200 | A09 | 51062988 | C | T | upstream_gene_variant | MODIFIER | c.-630C>T| |
S163 |
4 | BAA09g46200 | A09 | 51064529 | G | A | missense_variant | MODERATE | c.766G>A|p.Glu256Lys |
S187 |
5 | BAA09g46200 | A09 | 51064566 | C | T | missense_variant | MODERATE | c.803C>T|p.Thr268Ile |
S63 |
6 | BAA09g46200 | A09 | 51065024 | G | A | missense_variant | MODERATE | c.1055G>A|p.Arg352His |
S57 |
7 | BAA09g46200 | A09 | 51068869 | G | A | downstream_gene_variant | MODIFIER | c.*2895G>A| |
S47 |
8 | BAA09g46200 | A09 | 51069314 | C | T | downstream_gene_variant | MODIFIER | c.*3340C>T| |
S8 |
9 | BAA09g46200 | A09 | 51069383 | G | T | downstream_gene_variant | MODIFIER | c.*3409G>T| |
S106 S114 S125 S136 S146 S200 S217 S252 S267 S268 S289 S69 S81 |
10 | BAA09g46200 | A09 | 51069486 | C | T | downstream_gene_variant | MODIFIER | c.*3512C>T| |
S132 S137 S215 |
11 | BAA09g46200 | A09 | 51070594 | G | A | downstream_gene_variant | MODIFIER | c.*4620G>A| |
S127 |
12 | BAA09g46200 | A09 | 51070636 | C | T | downstream_gene_variant | MODIFIER | c.*4662C>T| |
S56 |