Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g06950 | A03 | 2911490 | C | T | upstream_gene_variant | MODIFIER | c.-4809C>T| |
S259 |
2 | BAA03g06950 | A03 | 2911525 | C | T | upstream_gene_variant | MODIFIER | c.-4774C>T| |
S232 |
3 | BAA03g06950 | A03 | 2911541 | G | A | upstream_gene_variant | MODIFIER | c.-4758G>A| |
S104 S52 |
4 | BAA03g06950 | A03 | 2918225 | C | T | missense_variant | MODERATE | c.563C>T|p.Ser188Leu |
S146 |
5 | BAA03g06950 | A03 | 2918497 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.655-1G>A| |
S122 |
6 | BAA03g06950 | A03 | 2918644 | C | T | intron_variant | MODIFIER | c.747+54C>T| |
S205 |
7 | BAA03g06950 | A03 | 2922574 | C | T | stop_gained&splice_region_variant | HIGH | c.1300C>T|p.Gln434* |
S171 |
8 | BAA03g06950 | A03 | 2922977 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.1375-1G>A| |
S149 S176 |
9 | BAA03g06950 | A03 | 2923070 | C | T | synonymous_variant | LOW | c.1467C>T|p.Asp489Asp |
S126 |
10 | BAA03g06950 | A03 | 2923713 | C | T | synonymous_variant | LOW | c.1815C>T|p.Tyr605Tyr |
S144 |