Product Details

SNP ID

rs11588547

Assay Type

Functionally tested

NCBI dbSNP Submissions

14

Location

Chr.1:160406305 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GCTCATTATTGCCTTTAATCTTGCA[C/T]TTGAGTAATTCCCCTGTTTTCTGAA

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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