Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g40980 | A09 | 47879289 | T | G | downstream_gene_variant | MODIFIER | c.*4129A>C| |
S296 |
2 | BAA09g40980 | A09 | 47879779 | G | A | downstream_gene_variant | MODIFIER | c.*3639C>T| |
S2 |
3 | BAA09g40980 | A09 | 47880235 | G | A | downstream_gene_variant | MODIFIER | c.*3183C>T| |
S281 |
4 | BAA09g40980 | A09 | 47881176 | G | A | downstream_gene_variant | MODIFIER | c.*2242C>T| |
S161 S97 |
5 | BAA09g40980 | A09 | 47882357 | G | A | downstream_gene_variant | MODIFIER | c.*1061C>T| |
S148 |
6 | BAA09g40980 | A09 | 47882369 | G | A | downstream_gene_variant | MODIFIER | c.*1049C>T| |
S189 |
7 | BAA09g40980 | A09 | 47883862 | C | T | synonymous_variant | LOW | c.465G>A|p.Thr155Thr |
S67 |
8 | BAA09g40980 | A09 | 47883879 | C | T | missense_variant | MODERATE | c.448G>A|p.Glu150Lys |
S256 |
9 | BAA09g40980 | A09 | 47884215 | C | T | missense_variant | MODERATE | c.112G>A|p.Glu38Lys |
S80 |
10 | BAA09g40980 | A09 | 47885033 | C | T | upstream_gene_variant | MODIFIER | c.-707G>A| |
S104 S52 |
11 | BAA09g40980 | A09 | 47885050 | C | T | upstream_gene_variant | MODIFIER | c.-724G>A| |
S205 |
12 | BAA09g40980 | A09 | 47885247 | C | T | upstream_gene_variant | MODIFIER | c.-921G>A| |
S6 |
13 | BAA09g40980 | A09 | 47885299 | G | A | upstream_gene_variant | MODIFIER | c.-973C>T| |
S156 |
14 | BAA09g40980 | A09 | 47886622 | C | T | upstream_gene_variant | MODIFIER | c.-2296G>A| |
S94 |
15 | BAA09g40980 | A09 | 47886722 | G | A | upstream_gene_variant | MODIFIER | c.-2396C>T| |
S149 |
16 | BAA09g40980 | A09 | 47888067 | C | T | upstream_gene_variant | MODIFIER | c.-3741G>A| |
S235 |
17 | BAA09g40980 | A09 | 47888146 | C | T | upstream_gene_variant | MODIFIER | c.-3820G>A| |
S121 |