Product Details

SNP ID

rs201198087

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:117278264 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGCGCAGCACCAGTGGAACTTACAC[C/T]CACACTTGGTCATCCGGGTGACATG

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	1274	Missense Mutation	GAG,GGG	E325G	NP_003382.1

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