Product Details

SNP ID

rs202058429

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.22:45923147 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCTGATAGCTGCGCAGCTGTTTGAT[A/G]CGCAGGAAGGTGGGCTGCCGCAGAC

Phenotype

MIM: 601967

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

WNT7B PubMed Links

Gene Details

Gene

WNT7B

Gene Name

Wnt family member 7B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_058238.2	1133	Silent Mutation	CGC,CGT	R253R	NP_478679.1
XM_011530366.1	1133	Silent Mutation	CGC,CGT	R257R	XP_011528668.1

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