Product Details

SNP ID

rs146457750

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:46769823 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTTGTTGTGCTTGTTCATGGCCGAG[C/T]GCGCGTCCGGCCTGTTCTCGCGCGC

Phenotype

MIM: 165330

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

WNT3 PubMed Links

Gene Details

Gene

WNT3

Gene Name

Wnt family member 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_030753.4	711	Missense Mutation	CAC,CGC	H183R	NP_110380.1

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