Product Details

SNP ID
hCV12075047
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.15:82811330 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATCTTCAACTTTATCGTCTTCACCT[T/G]AGGATATGAGGAACCCACAGGGGAG
Phenotype
MIM: 612393
Polymorphism
T/G, Transversion Substitution
Allele Nomenclature
Literature Links
FSD2 PubMed Links
Additional Information
For this assay, SNP(s) [rs142681702,rs145800406] 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
FSD2
Gene Name
fibronectin type III and SPRY domain containing 2
There are no transcripts associated with this gene.

Gene
WHAMM
Gene Name
WAS protein homolog associated with actin, golgi membranes and microtubules
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001080435.2 Intron NP_001073904.1

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