Product Details

SNP ID

rs200039404

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:73840110 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGAGGGCACCGACTATCAGCACCGC[G/T]TCGAAGGTCCCTGTGTGTGTGTGGG

Phenotype

MIM: 602909 MIM: 612546

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

CLDN4 PubMed Links

Gene Details

Gene

CLDN4

Gene Name

claudin 4

There are no transcripts associated with this gene.

Gene

WBSCR27

Gene Name

Williams Beuren syndrome chromosome region 27

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_152559.2	441	Missense Mutation	GAA,GAC	E133D	NP_689772.2
XM_017011777.1	441	Missense Mutation	GAA,GAC	E133D	XP_016867266.1
XM_017011778.1	441	Missense Mutation	GAA,GAC	E133D	XP_016867267.1

View Full Product Details