Product Details

SNP ID
rs4282179
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.4:104472163 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACATTATTTTTATGTCTTTTTCTTT[C/T]CTTTTCCTCTTTTTTTTTTTTTTTG
Phenotype
MIM: 611645
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
CXXC4 PubMed Links
Additional Information
For this assay, SNP(s) [rs34493088] are located under a probe 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
CXXC4
Gene Name
CXXC finger protein 4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_025212.3 1863 UTR 3 NP_079488.2
XM_011532284.2 1863 UTR 3 XP_011530586.1
XM_017008652.1 1863 UTR 3 XP_016864141.1

View Full Product Details