Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g08990 | A10 | 11076304 | G | A | upstream_gene_variant | MODIFIER | c.-3490G>A| |
S45 |
2 | BAA10g08990 | A10 | 11076370 | G | A | upstream_gene_variant | MODIFIER | c.-3424G>A| |
S184 |
3 | BAA10g08990 | A10 | 11076572 | G | A | upstream_gene_variant | MODIFIER | c.-3222G>A| |
S182 |
4 | BAA10g08990 | A10 | 11077235 | C | T | upstream_gene_variant | MODIFIER | c.-2559C>T| |
S199 |
5 | BAA10g08990 | A10 | 11077249 | G | A | upstream_gene_variant | MODIFIER | c.-2545G>A| |
S105 S106 |
6 | BAA10g08990 | A10 | 11080141 | G | A | splice_region_variant&intron_variant | LOW | c.149+5G>A| |
S32 |
7 | BAA10g08990 | A10 | 11080442 | G | A | missense_variant | MODERATE | c.298G>A|p.Glu100Lys |
S219 S72 |
8 | BAA10g08990 | A10 | 11080474 | C | T | synonymous_variant | LOW | c.330C>T|p.Phe110Phe |
S282 |
9 | BAA10g08990 | A10 | 11080514 | C | T | synonymous_variant | LOW | c.370C>T|p.Leu124Leu |
S275 |