Product Details

SNP ID

rs3767283

Assay Type

Functionally Tested

NCBI dbSNP Submissions

32

Location

Chr.1:205049133 on Build GRCh38

Set Membership

HapMap JSNP

Context Sequence [VIC/FAM]

GGAGGGTACCCAGGATCCCTGGGCC[A/G]GATTATTCGTGATTACCCATGGTAA

Phenotype

MIM: 190197

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

CNTN2 PubMed Links

Additional Information

For this assay, SNP(s) [rs79038900] 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

CNTN2

Gene Name

contactin 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005076.3		Intron			NP_005067.1
XM_017002198.1		Intron			XP_016857687.1
XM_017002199.1		Intron			XP_016857688.1

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