Product Details

SNP ID

rs149948419

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:73769800 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AAGGCGGCCAGCAGGATGGCCACCA[C/G]GATGAGGGCGCGGGCCGCCTGAAGG

Phenotype

MIM: 602910

Polymorphism

C/G, 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	471	Missense Mutation	CTG,GTG	L84V	NP_001297.1

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