Product Details

SNP ID
rs191204435
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.14:63599190 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGTTCAAACGTGTAACTGGTTCATC[A/G]GTGTCCAGATGATTAAGATCCCACC
Phenotype
Polymorphism
A/G, 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 1515 Silent Mutation ACC,ACT T251T NP_001008726.1
NM_001258272.1 1515 Silent Mutation ACC,ACT T251T NP_001245201.1
NM_080666.3 1515 Silent Mutation ACC,ACT T251T NP_542397.1
XM_011536383.2 1515 Silent Mutation ACC,ACT T289T XP_011534685.1
XM_011536385.2 1515 Silent Mutation ACC,ACT T251T XP_011534687.1

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