Product Details

SNP ID
rs200807787
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:117278164 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTGACGCCTGCTGGGGTCATGTAGC[A/G]GTTGTCCAGTCAGCGTTCTTGGGGG
Phenotype
MIM: 147870
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
WNT2 PubMed Links

Gene Details

Gene
WNT2
Gene Name
Wnt family member 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_003391.2 1374 Silent Mutation ACC,ACT T358T NP_003382.1

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