Product Details

SNP ID
rs202232294
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.22:45922979 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACTGGTGGGTGTTGTAGCCTCGGCC[A/G]CAGCACATGGTGTCACAGCCGTCCG
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 1301 Silent Mutation TGC,TGT C309C NP_478679.1
XM_011530366.1 1301 Silent Mutation TGC,TGT C313C XP_011528668.1

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