Product Details

SNP ID
rs201477654
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.7:73831708 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTGCCTCGCTCTACGTCGGCTGGGC[C/T]GCCTCCGGCCTGCTGCTCCTTGGCG
Phenotype
MIM: 602909 MIM: 612546
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
CLDN4 PubMed Links

Gene Details

Gene
CLDN4
Gene Name
claudin 4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001305.4 846 Silent Mutation GCC,GCT A169A NP_001296.1
Gene
WBSCR27
Gene Name
Williams Beuren syndrome chromosome region 27
There are no transcripts associated with this gene.

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