Product Details

SNP ID

rs35261626

Assay Type

Functionally tested

NCBI dbSNP Submissions

37

Location

Chr.1:205043956 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GAGTGGAGCACAAGTTTGGGCAAGG[G/T]CCTGTCCAGGAACTGGGACTCGGGG

Phenotype

MIM: 190197

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

CNTN2 PubMed Links

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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