Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g22690 | A10 | 19397781 | G | A | upstream_gene_variant | MODIFIER | c.-1419G>A| |
S4 |
2 | BAA10g22690 | A10 | 19399216 | C | T | missense_variant | MODERATE | c.17C>T|p.Thr6Ile |
S237 |
3 | BAA10g22690 | A10 | 19401241 | C | T | missense_variant | MODERATE | c.800C>T|p.Ala267Val |
S51 |
4 | BAA10g22690 | A10 | 19401665 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.1019-1G>A| |
S67 |