Product Details

SNP ID
rs2369608
Assay Type
Functionally Tested
NCBI dbSNP Submissions
44
Location
Chr.1:160407709 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
AGTGTACAGGACACTCACTGACTTA[C/T]GGGTCAGCACAACTCACCCACCTCC
Phenotype
MIM: 600533
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
VANGL2 PubMed Links

Gene Details

Gene
VANGL2
Gene Name
VANGL planar cell polarity protein 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_020335.2 Intron NP_065068.1
XM_005245357.1 Intron XP_005245414.1
XM_011509804.1 Intron XP_011508106.1
XM_011509805.2 Intron XP_011508107.1

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