Product Details

SNP ID

rs2976649

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.8:144802931 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GACCCTGGAATGGCGATGGCACTCC[C/T]GATGCCTGGACCTCAGGTGAGCACC

Phenotype

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

ZNF517 PubMed Links

Additional Information

For this assay, SNP(s) [rs113512121] 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

ZNF517

Gene Name

zinc finger protein 517

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001317936.1	663	Missense Mutation	CCG,CTG	P6L	NP_001304865.1
NM_213605.2	663	Missense Mutation	CCG,CTG	P6L	NP_998770.2
XM_011517014.2	663	Missense Mutation	CCG,CTG	P6L	XP_011515316.1
XM_011517015.2	663	Missense Mutation	CCG,CTG	P6L	XP_011515317.1
XM_011517017.2	663	Silent Mutation	CCC,CCT	P26P	XP_011515319.1
XM_017013384.1	663	Intron			XP_016868873.1

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