Product Details

SNP ID
rs147523002
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.14:63599120 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGATATAGGCCACCAATCAAATAGT[C/T]CAAAGCATCTTCTTTCATGTTAACT
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 1585 Missense Mutation AAC,GAC N275D NP_001008726.1
NM_001258272.1 1585 Missense Mutation AAC,GAC N275D NP_001245201.1
NM_080666.3 1585 Missense Mutation AAC,GAC N275D NP_542397.1
XM_011536383.2 1585 Missense Mutation AAC,GAC N313D XP_011534685.1
XM_011536385.2 1585 Missense Mutation AAC,GAC N275D XP_011534687.1

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