Product Details

SNP ID
rs12564690
Assay Type
Functionally tested
NCBI dbSNP Submissions
17
Location
Chr.1:200741948 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CTTTCCTACTATCACAGTGTTAGTA[A/G]GTGGCAGAAGTGAGTTTTGATTTGA
Phenotype
MIM: 613775
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
CAMSAP2 PubMed Links

Gene Details

Gene
CAMSAP2
Gene Name
calmodulin regulated spectrin associated protein family member 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001297707.1 Intron NP_001284636.1
NM_001297708.1 Intron NP_001284637.1
NM_203459.2 Intron NP_982284.1
XM_005245041.3 Intron XP_005245098.1
XM_017000799.1 Intron XP_016856288.1

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