Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g09150 | A03 | 3782135 | G | A | upstream_gene_variant | MODIFIER | c.-4406G>A| |
S25 S264 |
2 | BAA03g09150 | A03 | 3782671 | C | T | upstream_gene_variant | MODIFIER | c.-3870C>T| |
S209 |
3 | BAA03g09150 | A03 | 3782714 | G | A | upstream_gene_variant | MODIFIER | c.-3827G>A| |
S187 |
4 | BAA03g09150 | A03 | 3782738 | A | G | upstream_gene_variant | MODIFIER | c.-3803A>G| |
S95 |
5 | BAA03g09150 | A03 | 3782888 | C | T | upstream_gene_variant | MODIFIER | c.-3653C>T| |
S42 |
6 | BAA03g09150 | A03 | 3783113 | G | A | upstream_gene_variant | MODIFIER | c.-3428G>A| |
S176 |
7 | BAA03g09150 | A03 | 3783593 | G | A | upstream_gene_variant | MODIFIER | c.-2948G>A| |
S168 |
8 | BAA03g09150 | A03 | 3787837 | C | T | synonymous_variant | LOW | c.663C>T|p.Asn221Asn |
S278 |
9 | BAA03g09150 | A03 | 3788260 | T | C | synonymous_variant | LOW | c.894T>C|p.Arg298Arg |
S212 |
10 | BAA03g09150 | A03 | 3788716 | C | T | missense_variant | MODERATE | c.1165C>T|p.Leu389Phe |
S283 |
11 | BAA03g09150 | A03 | 3789032 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.1197-1G>A| |
S178 |
12 | BAA03g09150 | A03 | 3789073 | C | T | synonymous_variant | LOW | c.1237C>T|p.Leu413Leu |
S15 S3 |
13 | BAA03g09150 | A03 | 3789311 | C | T | downstream_gene_variant | MODIFIER | c.*32C>T| |
S247 |