Product Details

SNP ID
rs78748271
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:37886164 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTTAATATGTGGGACATAAATGGGG[C/T]CTTTAAGTCCTGTGCTTGGGACTCC
Phenotype
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
WDR87 PubMed Links

Gene Details

Gene
WDR87
Gene Name
WD repeat domain 87
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001291088.1 7761 Missense Mutation ACC,GCC T2503A NP_001278017.1
NM_031951.4 7761 Missense Mutation ACC,GCC T2464A NP_114157.4
XM_011527360.2 7761 Missense Mutation ACC,GCC T2503A XP_011525662.1

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