Product Details

SNP ID

rs34658204

Assay Type

Functionally Tested

NCBI dbSNP Submissions

22

Location

Chr.1:228016574 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGGAGGCTGTCCAGGGTCTGTGTGA[C/T]TTGCGCCATTTATCTCTGACTCATT

Phenotype

MIM: 606359

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

WNT3A PubMed Links

Additional Information

For this assay, SNP(s) [rs117195173] are located under a primer 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

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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