Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g32450 | A09 | 41127855 | C | T | downstream_gene_variant | MODIFIER | c.*4791G>A| |
S202 |
2 | BAA09g32450 | A09 | 41128796 | C | T | downstream_gene_variant | MODIFIER | c.*3850G>A| |
S205 |
3 | BAA09g32450 | A09 | 41128986 | C | T | downstream_gene_variant | MODIFIER | c.*3660G>A| |
S236 |
4 | BAA09g32450 | A09 | 41129259 | G | A | downstream_gene_variant | MODIFIER | c.*3387C>T| |
S126 |
5 | BAA09g32450 | A09 | 41129574 | C | T | downstream_gene_variant | MODIFIER | c.*3072G>A| |
S164 |
6 | BAA09g32450 | A09 | 41130602 | C | T | downstream_gene_variant | MODIFIER | c.*2044G>A| |
S30 S31 |
7 | BAA09g32450 | A09 | 41131779 | C | T | downstream_gene_variant | MODIFIER | c.*867G>A| |
S182 |
8 | BAA09g32450 | A09 | 41132301 | C | T | downstream_gene_variant | MODIFIER | c.*345G>A| |
S36 |
9 | BAA09g32450 | A09 | 41132527 | C | T | downstream_gene_variant | MODIFIER | c.*119G>A| |
S25 S264 |
10 | BAA09g32450 | A09 | 41132915 | G | A | missense_variant | MODERATE | c.1480C>T|p.Leu494Phe |
S270 |
11 | BAA09g32450 | A09 | 41134058 | G | A | missense_variant | MODERATE | c.431C>T|p.Thr144Met |
S59 |
12 | BAA09g32450 | A09 | 41135064 | C | T | upstream_gene_variant | MODIFIER | c.-576G>A| |
S275 |
13 | BAA09g32450 | A09 | 41136037 | C | T | upstream_gene_variant | MODIFIER | c.-1549G>A| |
S114 |
14 | BAA09g32450 | A09 | 41138525 | G | A | upstream_gene_variant | MODIFIER | c.-4037C>T| |
S71 |
15 | BAA09g32450 | A09 | 41138919 | C | T | upstream_gene_variant | MODIFIER | c.-4431G>A| |
S180 |