Product Details

SNP ID
rs150861119
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:37885212 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTCGTAGATGATCTCTTGGGGTTGA[A/G]GTTCCTCTCTCATTAGCAGCTCCTG
Phenotype
Polymorphism
A/G, 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 8713 Missense Mutation CCT,CTT P2820L NP_001278017.1
NM_031951.4 8713 Missense Mutation CCT,CTT P2781L NP_114157.4
XM_011527360.2 8713 Missense Mutation CCT,CTT P2820L XP_011525662.1

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