Product Details

SNP ID
rs79719688
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.17:46846292 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTCAGGTCTGACCTTCCACAGTCCA[A/G]TGTTTATTCATTCAGTTATTCATTC
Phenotype
MIM: 602864
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
WNT9B PubMed Links

Gene Details

Gene
WNT9B
Gene Name
Wnt family member 9B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001320458.1 Intron NP_001307387.1
NM_003396.2 Intron NP_003387.1
XM_011525178.2 Intron XP_011523480.1

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