Product Details
- SNP ID
-
rs151081297
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.7:73831262 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GCTGGCCGTCCTGGGCTGGCTGGCC[A/G]TCATGCTGTGCTGCGCGCTGCCCAT
- Phenotype
-
MIM: 602909
MIM: 612546
- Polymorphism
- A/G, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
CLDN4
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs8629] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.
Gene Details
- Gene
- CLDN4
- Gene Name
- claudin 4
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001305.4 |
400 |
Missense Mutation |
ATC,GTC |
I21V |
NP_001296.1 |
- Gene
- WBSCR27
- Gene Name
- Williams Beuren syndrome chromosome region 27
There are no transcripts associated with this gene.
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