Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g04990 | A05 | 2421356 | C | T | upstream_gene_variant | MODIFIER | c.-3966C>T| |
S59 |
2 | BAA05g04990 | A05 | 2421376 | C | T | upstream_gene_variant | MODIFIER | c.-3946C>T| |
S160 |
3 | BAA05g04990 | A05 | 2421402 | G | A | upstream_gene_variant | MODIFIER | c.-3920G>A| |
S279 |
4 | BAA05g04990 | A05 | 2423463 | C | T | upstream_gene_variant | MODIFIER | c.-1859C>T| |
S287 |
5 | BAA05g04990 | A05 | 2423627 | G | A | upstream_gene_variant | MODIFIER | c.-1695G>A| |
S206 S26 |
6 | BAA05g04990 | A05 | 2424272 | C | T | upstream_gene_variant | MODIFIER | c.-1050C>T| |
S51 |
7 | BAA05g04990 | A05 | 2424963 | C | T | upstream_gene_variant | MODIFIER | c.-359C>T| |
S184 |
8 | BAA05g04990 | A05 | 2424980 | G | A | upstream_gene_variant | MODIFIER | c.-342G>A| |
S265 |
9 | BAA05g04990 | A05 | 2425201 | C | T | upstream_gene_variant | MODIFIER | c.-121C>T| |
S288 |
10 | BAA05g04990 | A05 | 2425347 | C | T | missense_variant | MODERATE | c.26C>T|p.Ser9Leu |
S169 |
11 | BAA05g04990 | A05 | 2425556 | G | A | missense_variant | MODERATE | c.235G>A|p.Glu79Lys |
S133 |
12 | BAA05g04990 | A05 | 2425622 | C | T | missense_variant | MODERATE | c.301C>T|p.Pro101Ser |
S157 |
13 | BAA05g04990 | A05 | 2425751 | G | A | missense_variant | MODERATE | c.430G>A|p.Asp144Asn |
S302 |
14 | BAA05g04990 | A05 | 2426732 | G | A | downstream_gene_variant | MODIFIER | c.*712G>A| |
S242 |