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


Gene ID

Results: 1 - 21 of 21 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA10g19520 A10 17867395 C T downstream_gene_variant MODIFIER c.*4909G>A| S68
2 BAA10g19520 A10 17870024 G A downstream_gene_variant MODIFIER c.*2280C>T| S261
3 BAA10g19520 A10 17870237 C T downstream_gene_variant MODIFIER c.*2067G>A| S25
4 BAA10g19520 A10 17870651 G A downstream_gene_variant MODIFIER c.*1653C>T| S158
5 BAA10g19520 A10 17870808 G A downstream_gene_variant MODIFIER c.*1496C>T| S250
6 BAA10g19520 A10 17871202 G A downstream_gene_variant MODIFIER c.*1102C>T| S270
7 BAA10g19520 A10 17871538 G A downstream_gene_variant MODIFIER c.*766C>T| S240
8 BAA10g19520 A10 17872175 C T downstream_gene_variant MODIFIER c.*129G>A| S186
9 BAA10g19520 A10 17872224 C T downstream_gene_variant MODIFIER c.*80G>A| S83
S88
10 BAA10g19520 A10 17872248 G A downstream_gene_variant MODIFIER c.*56C>T| S174
S27
11 BAA10g19520 A10 17872666 C T missense_variant MODERATE c.289G>A|p.Asp97Asn S157
12 BAA10g19520 A10 17872711 C T intron_variant MODIFIER c.274-30G>A| S114
13 BAA10g19520 A10 17872723 C T intron_variant MODIFIER c.274-42G>A| S282
14 BAA10g19520 A10 17874059 G A intron_variant MODIFIER c.274-1378C>T| S132
S137
S215
S288
S89
15 BAA10g19520 A10 17876761 C T missense_variant MODERATE c.208G>A|p.Glu70Lys S127
16 BAA10g19520 A10 17877012 G A missense_variant MODERATE c.35C>T|p.Ala12Val S112
17 BAA10g19520 A10 17877343 G T upstream_gene_variant MODIFIER c.-56C>A| S236
18 BAA10g19520 A10 17877467 C T upstream_gene_variant MODIFIER c.-180G>A| S172
S247
19 BAA10g19520 A10 17878290 G A upstream_gene_variant MODIFIER c.-1003C>T| S273
20 BAA10g19520 A10 17880462 C T upstream_gene_variant MODIFIER c.-3175G>A| S183
21 BAA10g19520 A10 17881549 G A upstream_gene_variant MODIFIER c.-4262C>T| S139