Product Details

SNP ID
rs138008896
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.21:36461032 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGCGTGGCCGAGGTCACTGAGGGGG[C/T]CCGATTGTCTTTGTAGGCAGCTGGT
Phenotype
MIM: 605608
Polymorphism
C/T, Transition 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 1138 Missense Mutation NP_001139549.1
NM_001146078.2 1138 Missense Mutation NP_001139550.1
NM_001146079.1 1138 Missense Mutation NP_001139551.1
NM_012130.3 1138 Missense Mutation NP_036262.1
NM_144492.2 1138 Missense Mutation NP_652763.1

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