Product Details

SNP ID
rs3747548
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:45847462 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTCCACGTCGCCTACCGGGGCGGAG[A/C]GGGGGTGGCTGGAGCAGTCTGGACA
Phenotype
MIM: 603732
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
CRY2 PubMed Links

Gene Details

Gene
CRY2
Gene Name
cryptochrome circadian clock 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001127457.2 57 Intron NP_001120929.1
NM_021117.3 57 Missense Mutation GAG,GCG E12A NP_066940.2

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