Product Details

SNP ID

rs9856296

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.3:14113953 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTCACATCTAAATAGTATTTCTTGG[C/T]TTTCCAAAATGCTCTCAAAACGATG

Phenotype

MIM: 611077

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

CHCHD4 PubMed Links

Additional Information

For this assay, SNP(s) [rs77997750] are located under a probe and SNP(s) [rs116195395] 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

CHCHD4

Gene Name

coiled-coil-helix-coiled-coil-helix domain containing 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001098502.1		Intron			NP_001091972.1
NM_144636.2		Intron			NP_653237.1

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