Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g01790 | A04 | 1040984 | G | A | splice_region_variant&intron_variant | LOW | c.478-4C>T| |
S144 |
2 | BAA04g01790 | A04 | 1041687 | G | A | synonymous_variant | LOW | c.198C>T|p.His66His |
S289 |
3 | BAA04g01790 | A04 | 1041826 | C | T | missense_variant | MODERATE | c.59G>A|p.Gly20Asp |
S135 |
4 | BAA04g01790 | A04 | 1043394 | G | A | upstream_gene_variant | MODIFIER | c.-1510C>T| |
S161 |
5 | BAA04g01790 | A04 | 1043736 | G | A | upstream_gene_variant | MODIFIER | c.-1852C>T| |
S183 S198 |
6 | BAA04g01790 | A04 | 1045097 | C | T | upstream_gene_variant | MODIFIER | c.-3213G>A| |
S206 S26 |
7 | BAA04g01790 | A04 | 1045126 | C | T | upstream_gene_variant | MODIFIER | c.-3242G>A| |
S293 |