Product Details

SNP ID
rs199577372
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.7:73834932 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCCCAGCCTGCTCCAGCCTGTCCAG[C/G]GTGGCCTCCAGAGCCTCCTTGTATT
Phenotype
MIM: 602909 MIM: 612546
Polymorphism
C/G, Transversion Substitution
Allele Nomenclature
Literature Links
CLDN4 PubMed Links

Gene Details

Gene
CLDN4
Gene Name
claudin 4
There are no transcripts associated with this gene.

Gene
WBSCR27
Gene Name
Williams Beuren syndrome chromosome region 27
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_152559.2 669 Silent Mutation ACC,ACG T183T NP_689772.2
XM_017011777.1 669 Silent Mutation ACC,ACG T209T XP_016867266.1
XM_017011778.1 669 Silent Mutation ACC,ACG T209T XP_016867267.1

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