Product Details

SNP ID

rs201026179

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:117278287 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACCCACACTTGGTCATCCGGGTGAC[A/G]TGGGAGGTGTCGTAGCCTCTCCCAC

Phenotype

MIM: 147870

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

WNT2 PubMed Links

Gene Details

Gene

WNT2

Gene Name

Wnt family member 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_003391.2	1251	Silent Mutation	CAC,CAT	H317H	NP_003382.1

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