Product Details

SNP ID
rs12548737
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.8:8703026 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCGCAGCAGCGTCAGCACCATCCAA[A/G]TGGAGTGGCCCGAGCCCGACCTGGC
Phenotype
MIM: 609203
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
CLDN23 PubMed Links

Gene Details

Gene
CLDN23
Gene Name
claudin 23
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_194284.2 871 Missense Mutation ATG,GTG M210V NP_919260.2

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