Product Details

SNP ID
rs9990189
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:190390570 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GAAGAAGAAGAACCCTGTAACAAAT[C/G]CGGCTCCCTTCTCTTTCAACAATCT
Phenotype
MIM: 603959
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
CLDN16 PubMed Links

Gene Details

Gene
CLDN16
Gene Name
claudin 16
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_006580.3 Intron NP_006571.1

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