Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g25740 | A06 | 17645499 | G | A | upstream_gene_variant | MODIFIER | c.-2703G>A| |
S70 |
2 | BAA06g25740 | A06 | 17646541 | G | A | upstream_gene_variant | MODIFIER | c.-1661G>A| |
S89 |
3 | BAA06g25740 | A06 | 17646572 | G | A | upstream_gene_variant | MODIFIER | c.-1630G>A| |
S72 S78 |
4 | BAA06g25740 | A06 | 17646821 | G | A | upstream_gene_variant | MODIFIER | c.-1381G>A| |
S208 |
5 | BAA06g25740 | A06 | 17647568 | C | T | upstream_gene_variant | MODIFIER | c.-634C>T| |
S62 |
6 | BAA06g25740 | A06 | 17648530 | C | T | missense_variant | MODERATE | c.257C>T|p.Ser86Phe |
S228 |
7 | BAA06g25740 | A06 | 17649134 | C | T | splice_region_variant&intron_variant | LOW | c.646+6C>T| |
S296 |
8 | BAA06g25740 | A06 | 17649573 | G | A | missense_variant | MODERATE | c.868G>A|p.Gly290Ser |
S23 |
9 | BAA06g25740 | A06 | 17649592 | G | A | missense_variant | MODERATE | c.887G>A|p.Gly296Glu |
S283 |
10 | BAA06g25740 | A06 | 17649753 | G | A | intron_variant | MODIFIER | c.972+76G>A| |
S41 |
11 | BAA06g25740 | A06 | 17655552 | C | T | downstream_gene_variant | MODIFIER | c.*4810C>T| |
S288 |