Product Details

SNP ID
rs113016282
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:73769988 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCACATGGGCAACGCGCAGCACACG[A/G]TGGTGCCCAGCCAGCCCAGCACGGC
Phenotype
MIM: 602910
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
CLDN3 PubMed Links

Gene Details

Gene
CLDN3
Gene Name
claudin 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001306.3 283 Missense Mutation ACC,ATC T21I NP_001297.1

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