Product Details
- SNP ID
-
rs691878
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.7:49855506 on Build GRCh38
- Set Membership
-
HapMap
- Context Sequence [VIC/FAM]
- TTCCCAGGTGAAAGAGGACAGATGT[C/T]GTGGAGAGAGGTAAGGAAGGCTCAG
- Phenotype
-
MIM: 611108
MIM: 608498
- Polymorphism
- C/T, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
VWC2
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs79368066] 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
- VWC2
- Gene Name
- von Willebrand factor C domain containing 2
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_198570.4 |
|
Intron |
|
|
NP_940972.2 |
- Gene
- ZPBP
- Gene Name
- zona pellucida binding protein
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