Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g30740 | A04 | 29117254 | G | A | downstream_gene_variant | MODIFIER | c.*1753C>T| |
S289 S290 |
2 | BAA04g30740 | A04 | 29119182 | C | T | missense_variant&splice_region_variant | MODERATE | c.1774G>A|p.Ala592Thr |
S250 |
3 | BAA04g30740 | A04 | 29120118 | G | A | missense_variant | MODERATE | c.1151C>T|p.Thr384Ile |
S183 |
4 | BAA04g30740 | A04 | 29120965 | G | A | missense_variant | MODERATE | c.605C>T|p.Thr202Ile |
S51 |
5 | BAA04g30740 | A04 | 29122675 | G | A | upstream_gene_variant | MODIFIER | c.-436C>T| |
S60 |
6 | BAA04g30740 | A04 | 29123558 | C | T | upstream_gene_variant | MODIFIER | c.-1319G>A| |
S107 |
7 | BAA04g30740 | A04 | 29124156 | C | T | upstream_gene_variant | MODIFIER | c.-1917G>A| |
S291 |
8 | BAA04g30740 | A04 | 29125956 | C | T | upstream_gene_variant | MODIFIER | c.-3717G>A| |
S297 |
9 | BAA04g30740 | A04 | 29127053 | C | T | upstream_gene_variant | MODIFIER | c.-4814G>A| |
S216 |