Product Details

SNP ID
rs144371384
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.21:36461108 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CAGTGGTCGTGGTGGCCCTGGGCGG[G/T]GCCTGGTAGGGCCTGTAGGGTGCCT
Phenotype
MIM: 605608
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
CLDN14 PubMed Links

Gene Details

Gene
CLDN14
Gene Name
claudin 14
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001146077.1 1062 Silent Mutation NP_001139549.1
NM_001146078.2 1062 Silent Mutation NP_001139550.1
NM_001146079.1 1062 Silent Mutation NP_001139551.1
NM_012130.3 1062 Silent Mutation NP_036262.1
NM_144492.2 1062 Silent Mutation NP_652763.1

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