Product Details

SNP ID

rs165697

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.22:29481568 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGCTTCCCCGCCAATGCTGCCATGC[C/T]CTCTCCTACACCCCGCAAGAAACTC

Phenotype

MIM: 162230

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

NEFH PubMed Links

Additional Information

For this assay, SNP(s) [rs75956622] 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

NEFH

Gene Name

neurofilament heavy polypeptide

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_021076.3		Intron			NP_066554.2
XM_011530200.2		Intron			XP_011528502.1

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