Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g15820 | A01 | 7685856 | C | T | upstream_gene_variant | MODIFIER | c.-4943C>T| |
S210 S225 |
2 | BAA01g15820 | A01 | 7687633 | G | A | upstream_gene_variant | MODIFIER | c.-3166G>A| |
S129 |
3 | BAA01g15820 | A01 | 7687931 | C | T | upstream_gene_variant | MODIFIER | c.-2868C>T| |
S164 |
4 | BAA01g15820 | A01 | 7688088 | G | A | upstream_gene_variant | MODIFIER | c.-2711G>A| |
S40 |
5 | BAA01g15820 | A01 | 7688762 | G | A | upstream_gene_variant | MODIFIER | c.-2037G>A| |
S249 |
6 | BAA01g15820 | A01 | 7689688 | G | A | upstream_gene_variant | MODIFIER | c.-1111G>A| |
S199 |
7 | BAA01g15820 | A01 | 7690084 | G | A | upstream_gene_variant | MODIFIER | c.-715G>A| |
S72 S78 |
8 | BAA01g15820 | A01 | 7690135 | G | A | upstream_gene_variant | MODIFIER | c.-664G>A| |
S240 |
9 | BAA01g15820 | A01 | 7690197 | C | T | upstream_gene_variant | MODIFIER | c.-602C>T| |
S185 |
10 | BAA01g15820 | A01 | 7690956 | A | T | missense_variant | MODERATE | c.158A>T|p.Gln53Leu |
S143 |
11 | BAA01g15820 | A01 | 7690987 | C | T | synonymous_variant | LOW | c.189C>T|p.Arg63Arg |
S128 |
12 | BAA01g15820 | A01 | 7691009 | C | T | missense_variant | MODERATE | c.211C>T|p.Pro71Ser |
S182 |
13 | BAA01g15820 | A01 | 7691056 | G | A | intron_variant | MODIFIER | c.244+14G>A| |
S129 |
14 | BAA01g15820 | A01 | 7691178 | C | T | synonymous_variant | LOW | c.324C>T|p.Arg108Arg |
S182 |
15 | BAA01g15820 | A01 | 7691275 | G | A | missense_variant | MODERATE | c.421G>A|p.Val141Ile |
S117 |
16 | BAA01g15820 | A01 | 7691640 | G | A | synonymous_variant | LOW | c.618G>A|p.Arg206Arg |
S92 |
17 | BAA01g15820 | A01 | 7691899 | G | A | missense_variant | MODERATE | c.793G>A|p.Val265Ile |
S306 S308 |