Product Details

SNP ID

rs202139199

Assay Type

Functionally Tested

NCBI dbSNP Submissions

3

Location

Chr.1:22120229 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTGGACGTCTTGTTGCATGTGCGGC[C/T]CCTCGTGCCCAGCACGCCGCTGCGC

Phenotype

MIM: 603490

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

WNT4 PubMed Links

Additional Information

For this assay, SNP(s) [rs34228276] 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

WNT4

Gene Name

Wnt family member 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_030761.4	1050	Missense Mutation	AGC,GGC	S293G	NP_110388.2
XM_011541597.2	1050	Missense Mutation	AGC,GGC	S315G	XP_011539899.1
XM_011541598.2	1050	Missense Mutation	AGC,GGC	S238G	XP_011539900.1
XM_011541599.1	1050	Intron			XP_011539901.1

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