Users can query the SNP information according to the gene ID.


Gene ID

Results: 1 - 15 of 15 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA10g10690 A10 12464925 C T upstream_gene_variant MODIFIER c.-1880C>T| S176
2 BAA10g10690 A10 12465737 G A upstream_gene_variant MODIFIER c.-1068G>A| S129
3 BAA10g10690 A10 12465894 G A upstream_gene_variant MODIFIER c.-911G>A| S4
4 BAA10g10690 A10 12466160 G A upstream_gene_variant MODIFIER c.-645G>A| S296
5 BAA10g10690 A10 12466411 G A upstream_gene_variant MODIFIER c.-394G>A| S138
6 BAA10g10690 A10 12466678 C T upstream_gene_variant MODIFIER c.-127C>T| S274
7 BAA10g10690 A10 12466837 C T synonymous_variant LOW c.33C>T|p.Ser11Ser S17
8 BAA10g10690 A10 12466985 G A splice_region_variant&intron_variant LOW c.92-5G>A| S303
9 BAA10g10690 A10 12467551 G A synonymous_variant LOW c.468G>A|p.Lys156Lys S55
10 BAA10g10690 A10 12467962 G A synonymous_variant LOW c.879G>A|p.Arg293Arg S198
11 BAA10g10690 A10 12468042 C T missense_variant MODERATE c.959C>T|p.Thr320Ile S20
12 BAA10g10690 A10 12468114 G A missense_variant MODERATE c.1031G>A|p.Arg344His S64
13 BAA10g10690 A10 12468512 C T missense_variant MODERATE c.1429C>T|p.Pro477Ser S186
14 BAA10g10690 A10 12468795 G A missense_variant MODERATE c.1712G>A|p.Arg571Lys S306
S308
15 BAA10g10690 A10 12470706 G A downstream_gene_variant MODIFIER c.*1796G>A| S130