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


Gene ID

Results: 1 - 489298 of 489298 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
135851 BAA10g21610 A10 18952904 C T upstream_gene_variant MODIFIER c.-4472G>A| S20
135852 BAA10g21610 A10 18953424 G A upstream_gene_variant MODIFIER c.-4992C>T| S178
135853 BAA10g21620 A10 18954257 G A upstream_gene_variant MODIFIER c.-2015C>T| S289
S290
135854 BAA10g21620 A10 18955119 C T upstream_gene_variant MODIFIER c.-2877G>A| S275
135855 BAA10g21620 A10 18955660 G A upstream_gene_variant MODIFIER c.-3418C>T| S36
135856 BAA10g21620 A10 18956097 G A upstream_gene_variant MODIFIER c.-3855C>T| S32
135857 BAA10g21620 A10 18956122 G A upstream_gene_variant MODIFIER c.-3880C>T| S59
135858 BAA10g21620 A10 18956201 G A upstream_gene_variant MODIFIER c.-3959C>T| S103
135859 BAA10g21620 A10 18956217 C T upstream_gene_variant MODIFIER c.-3975G>A| S238
135860 BAA10g21630 A10 18957025 C T missense_variant MODERATE c.266C>T|p.Pro89Leu S124
135861 BAA10g21640 A10 18957414 G A synonymous_variant LOW c.69G>A|p.Lys23Lys S109
135862 BAA10g21640 A10 18957935 C T missense_variant MODERATE c.280C>T|p.Pro94Ser S275
135863 BAA10g21640 A10 18958450 C T synonymous_variant LOW c.502C>T|p.Leu168Leu S168
135864 BAA10g21640 A10 18958471 C T missense_variant MODERATE c.523C>T|p.His175Tyr S161
135865 BAA10g21640 A10 18958648 C T missense_variant MODERATE c.700C>T|p.Leu234Phe S40
S49
135866 BAA10g21640 A10 18958820 C T missense_variant MODERATE c.872C>T|p.Thr291Ile S80
135867 BAA10g21650 A10 18961180 C T upstream_gene_variant MODIFIER c.-4085C>T| S156
135868 BAA10g21640 A10 18961500 C T missense_variant MODERATE c.3028C>T|p.Pro1010Ser S191
135869 BAA10g21640 A10 18961503 C T synonymous_variant LOW c.3031C>T|p.Leu1011Leu S47
135870 BAA10g21650 A10 18962937 G A upstream_gene_variant MODIFIER c.-2328G>A| S130
135871 BAA10g21650 A10 18963880 G A upstream_gene_variant MODIFIER c.-1385G>A| S167
135872 BAA10g21650 A10 18965097 C T upstream_gene_variant MODIFIER c.-168C>T| S23
135873 BAA10g21650 A10 18965442 G A missense_variant MODERATE c.178G>A|p.Asp60Asn S3
135874 BAA10g21650 A10 18965559 C T missense_variant MODERATE c.295C>T|p.Pro99Ser S47
135875 BAA10g21650 A10 18965638 C T missense_variant MODERATE c.374C>T|p.Ser125Leu S244