Product Details

SNP ID
rs699637
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.12:64189732 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GAAAGCTGGAAGGGCCATAAAAACA[C/T]TGGGCAAAATGGACTTTGGAGTAAG
Phenotype
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
C12orf66 PubMed Links

Gene Details

Gene
C12orf66
Gene Name
chromosome 12 open reading frame 66
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001300940.1 Intron NP_001287869.1
NM_001300941.1 Intron NP_001287870.1
NM_152440.4 Intron NP_689653.3

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