Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g19900 | A02 | 10450194 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.179-1G>A| |
S209 |
2 | BAA02g19900 | A02 | 10450692 | G | A | missense_variant | MODERATE | c.97C>T|p.Pro33Ser |
S159 S243 |
3 | BAA02g19900 | A02 | 10454971 | G | A | upstream_gene_variant | MODIFIER | c.-4183C>T| |
S247 |
4 | BAA02g19900 | A02 | 10455333 | G | A | upstream_gene_variant | MODIFIER | c.-4545C>T| |
S13 |
5 | BAA02g19900 | A02 | 10455353 | G | A | upstream_gene_variant | MODIFIER | c.-4565C>T| |
S166 |
6 | BAA02g19900 | A02 | 10455359 | C | T | upstream_gene_variant | MODIFIER | c.-4571G>A| |
S88 |