Product Details

SNP ID

rs201430959

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:121329681 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGAAACCGTACCTGCTGCCGAGCAT[C/T]CGAGAGGGCGCCCGGCTGGGCATTC

Phenotype

MIM: 606267

Polymorphism

C/T, Transition 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	467	Silent Mutation	ATC,ATT	I60I	NP_057171.2
NM_057168.1	467	Silent Mutation	ATC,ATT	I70I	NP_476509.1

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