Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g42670 | A09 | 48980113 | G | A | upstream_gene_variant | MODIFIER | c.-3272G>A| |
S38 |
2 | BAA09g42670 | A09 | 48980198 | G | A | upstream_gene_variant | MODIFIER | c.-3187G>A| |
S246 |
3 | BAA09g42670 | A09 | 48981271 | G | A | upstream_gene_variant | MODIFIER | c.-2114G>A| |
S115 |
4 | BAA09g42670 | A09 | 48981509 | G | A | upstream_gene_variant | MODIFIER | c.-1876G>A| |
S249 |
5 | BAA09g42670 | A09 | 48982367 | C | T | upstream_gene_variant | MODIFIER | c.-1018C>T| |
S95 |
6 | BAA09g42670 | A09 | 48982659 | G | A | upstream_gene_variant | MODIFIER | c.-726G>A| |
S115 |
7 | BAA09g42670 | A09 | 48982961 | C | T | upstream_gene_variant | MODIFIER | c.-424C>T| |
S280 |
8 | BAA09g42670 | A09 | 48983115 | C | T | upstream_gene_variant | MODIFIER | c.-270C>T| |
S182 |
9 | BAA09g42670 | A09 | 48983579 | C | T | intron_variant | MODIFIER | c.151-30C>T| |
S278 |
10 | BAA09g42670 | A09 | 48983667 | C | T | missense_variant | MODERATE | c.209C>T|p.Ala70Val |
S174 S18 |
11 | BAA09g42670 | A09 | 48984660 | C | T | intron_variant | MODIFIER | c.800+27C>T| |
S302 |
12 | BAA09g42670 | A09 | 48985157 | G | A | downstream_gene_variant | MODIFIER | c.*423G>A| |
S185 |
13 | BAA09g42670 | A09 | 48986091 | G | A | downstream_gene_variant | MODIFIER | c.*1357G>A| |
S188 |
14 | BAA09g42670 | A09 | 48986308 | C | T | downstream_gene_variant | MODIFIER | c.*1574C>T| |
S251 |
15 | BAA09g42670 | A09 | 48988063 | G | A | downstream_gene_variant | MODIFIER | c.*3329G>A| |
S167 |