Product Details

SNP ID

rs201719232

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:117278166 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GACGCCTGCTGGGGTCATGTAGCGG[C/T]TGTCCAGTCAGCGTTCTTGGGGGCC

Phenotype

MIM: 147870

Polymorphism

C/T, 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	1372	Missense Mutation	ACC,GCC	T358A	NP_003382.1

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