Product Details

SNP ID

rs200737615

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:121329751 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CAGACACGAGAGATGGAACTGCATG[A/T]TCACCGCCGCCGCCACTACCGCCCC

Phenotype

MIM: 606267

Polymorphism

A/T, Transversion substitution

Allele Nomenclature

Literature Links

WNT16 PubMed Links

Gene Details

Gene

WNT16

Gene Name

Wnt family member 16

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_016087.2	537	Missense Mutation	ATC,TTC	I84F	NP_057171.2
NM_057168.1	537	Missense Mutation	ATC,TTC	I94F	NP_476509.1

View Full Product Details