Product Details

SNP ID
rs200825628
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:73769761 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTGGTGCACTGGGCGCCCACCAGCG[A/C]CACTAGCAGCCCGAAGGCGGCCAGC
Phenotype
MIM: 602910
Polymorphism
A/C, Transversion 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_001306.3 510 Missense Mutation GCG,TCG A97S NP_001297.1

View Full Product Details