Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g12900 | A06 | 6455637 | G | A | upstream_gene_variant | MODIFIER | c.-3780G>A| |
S282 |
2 | BAA06g12900 | A06 | 6455854 | C | T | upstream_gene_variant | MODIFIER | c.-3563C>T| |
S115 |
3 | BAA06g12900 | A06 | 6456534 | C | T | upstream_gene_variant | MODIFIER | c.-2883C>T| |
S37 |
4 | BAA06g12900 | A06 | 6456867 | G | A | upstream_gene_variant | MODIFIER | c.-2550G>A| |
S5 |
5 | BAA06g12900 | A06 | 6458678 | G | A | upstream_gene_variant | MODIFIER | c.-739G>A| |
S182 |
6 | BAA06g12900 | A06 | 6461206 | C | T | synonymous_variant | LOW | c.307C>T|p.Leu103Leu |
S256 |
7 | BAA06g12900 | A06 | 6466129 | C | T | intron_variant | MODIFIER | c.417-267C>T| |
S2 |
8 | BAA06g12900 | A06 | 6466587 | G | A | splice_donor_variant&intron_variant | HIGH | c.607+1G>A| |
S191 |
9 | BAA06g12900 | A06 | 6469040 | C | T | missense_variant | MODERATE | c.1661C>T|p.Ala554Val |
S223 |