Product Details

SNP ID
rs202032576
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.14:63598867 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGATGCTATTTTCATACTCTCTTTC[C/T]TTGTAAAGGTCTTCTCTATAGCTCC
Phenotype
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
WDR89 PubMed Links

Gene Details

Gene
WDR89
Gene Name
WD repeat domain 89
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001008726.2 1838 Missense Mutation AAG,AGG K359R NP_001008726.1
NM_001258272.1 1838 Missense Mutation AAG,AGG K359R NP_001245201.1
NM_080666.3 1838 Missense Mutation AAG,AGG K359R NP_542397.1
XM_011536383.2 1838 Missense Mutation AAG,AGG K397R XP_011534685.1
XM_011536385.2 1838 Missense Mutation AAG,AGG K359R XP_011534687.1

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