Product Details

SNP ID
rs143165130
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.14:63599107 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTCTGTCTTTTCATGATATAGGCCA[C/T]CAATCAAATAGTCCAAAGCATCTTC
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 1598 Missense Mutation GAT,GGT D279G NP_001008726.1
NM_001258272.1 1598 Missense Mutation GAT,GGT D279G NP_001245201.1
NM_080666.3 1598 Missense Mutation GAT,GGT D279G NP_542397.1
XM_011536383.2 1598 Missense Mutation GAT,GGT D317G XP_011534685.1
XM_011536385.2 1598 Missense Mutation GAT,GGT D279G XP_011534687.1

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