Product Details

SNP ID

rs708114

Assay Type

Functionally tested

NCBI dbSNP Submissions

44

Location

Chr.1:228009795 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AGAGGCAAAGGTGTCCCTGTGGCCA[A/G]CAGCCCTGTGAGAGTGTGAAGGGCC

Phenotype

MIM: 606359

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

WNT3A PubMed Links

Gene Details

Gene

WNT3A

Gene Name

Wnt family member 3A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_033131.3		Intron			NP_149122.1
XM_011544319.2		Intron			XP_011542621.1

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