Product Details

SNP ID
rs11546416
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.7:56106408 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGGAGGTGCGGCTTCGGCTTCCACG[T/C]GGCATCCTAGGTAAGCGACGGCTAG
Phenotype
MIM: 616244
Polymorphism
T/C, Transition Substitution
Allele Nomenclature
Literature Links
CHCHD2 PubMed Links
Additional Information
For this assay, SNP(s) [rs10043] 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
CHCHD2
Gene Name
coiled-coil-helix-coiled-coil-helix domain containing 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001320327.1 Intron NP_001307256.1
NM_016139.3 Intron NP_057223.1
Gene
NUPR2
Gene Name
nuclear protein 2, transcriptional regulator
There are no transcripts associated with this gene.

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