Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g46470 | A09 | 51203763 | G | A | downstream_gene_variant | MODIFIER | c.*1188C>T| |
S289 S290 |
2 | BAA09g46470 | A09 | 51204445 | G | A | downstream_gene_variant | MODIFIER | c.*506C>T| |
S54 |
3 | BAA09g46470 | A09 | 51205394 | C | T | missense_variant | MODERATE | c.547G>A|p.Val183Ile |
S241 |
4 | BAA09g46470 | A09 | 51205815 | C | T | synonymous_variant | LOW | c.126G>A|p.Ser42Ser |
S52 |
5 | BAA09g46470 | A09 | 51206937 | G | A | upstream_gene_variant | MODIFIER | c.-997C>T| |
S111 |
6 | BAA09g46470 | A09 | 51207869 | C | T | upstream_gene_variant | MODIFIER | c.-1929G>A| |
S146 |
7 | BAA09g46470 | A09 | 51208736 | G | A | upstream_gene_variant | MODIFIER | c.-2796C>T| |
S42 |
8 | BAA09g46470 | A09 | 51209489 | G | A | upstream_gene_variant | MODIFIER | c.-3549C>T| |
S279 |
9 | BAA09g46470 | A09 | 51209923 | G | A | upstream_gene_variant | MODIFIER | c.-3983C>T| |
S231 |