Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g00020 | A03 | 10132 | C | T | upstream_gene_variant | MODIFIER | c.-3931C>T| |
S195 |
2 | BAA03g00020 | A03 | 10435 | C | T | upstream_gene_variant | MODIFIER | c.-3628C>T| |
S228 |
3 | BAA03g00020 | A03 | 10488 | G | A | upstream_gene_variant | MODIFIER | c.-3575G>A| |
S286 |
4 | BAA03g00020 | A03 | 10507 | G | A | upstream_gene_variant | MODIFIER | c.-3556G>A| |
S208 S93 |
5 | BAA03g00020 | A03 | 10886 | G | A | upstream_gene_variant | MODIFIER | c.-3177G>A| |
S13 |
6 | BAA03g00020 | A03 | 10928 | C | T | upstream_gene_variant | MODIFIER | c.-3135C>T| |
S251 |
7 | BAA03g00020 | A03 | 11773 | C | T | upstream_gene_variant | MODIFIER | c.-2290C>T| |
S180 |
8 | BAA03g00020 | A03 | 12558 | G | A | upstream_gene_variant | MODIFIER | c.-1505G>A| |
S274 |
9 | BAA03g00020 | A03 | 12964 | C | T | upstream_gene_variant | MODIFIER | c.-1099C>T| |
S163 |
10 | BAA03g00020 | A03 | 13298 | C | T | upstream_gene_variant | MODIFIER | c.-765C>T| |
S171 |
11 | BAA03g00020 | A03 | 14324 | G | A | missense_variant | MODERATE | c.262G>A|p.Asp88Asn |
S213 |