Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g06690 | A10 | 3580744 | C | T | downstream_gene_variant | MODIFIER | c.*367G>A| |
S37 |
2 | BAA10g06690 | A10 | 3581362 | G | A | missense_variant | MODERATE | c.1000C>T|p.His334Tyr |
S19 |
3 | BAA10g06690 | A10 | 3581774 | G | A | intron_variant | MODIFIER | c.846-258C>T| |
S134 |
4 | BAA10g06690 | A10 | 3582256 | C | T | intron_variant | MODIFIER | c.845+323G>A| |
S35 |
5 | BAA10g06690 | A10 | 3582837 | G | A | intron_variant | MODIFIER | c.721-134C>T| |
S182 |
6 | BAA10g06690 | A10 | 3583348 | G | A | intron_variant | MODIFIER | c.502-19C>T| |
S20 |
7 | BAA10g06690 | A10 | 3583799 | C | T | synonymous_variant | LOW | c.264G>A|p.Ser88Ser |
S247 |
8 | BAA10g06690 | A10 | 3584047 | C | T | missense_variant | MODERATE | c.16G>A|p.Val6Ile |
S294 |
9 | BAA10g06690 | A10 | 3584564 | C | T | upstream_gene_variant | MODIFIER | c.-502G>A| |
S263 |
10 | BAA10g06690 | A10 | 3585522 | G | A | upstream_gene_variant | MODIFIER | c.-1460C>T| |
S184 |
11 | BAA10g06690 | A10 | 3586475 | G | A | upstream_gene_variant | MODIFIER | c.-2413C>T| |
S245 |
12 | BAA10g06690 | A10 | 3586675 | G | A | upstream_gene_variant | MODIFIER | c.-2613C>T| |
S179 |