Product Details

SNP ID
rs144369996
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.X:118346557 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCTATGATGCCCCTGAAGATGTGCA[C/T]CTAGGGGGCGGCTACCCCGTGGGGT
Phenotype
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
WDR44 PubMed Links

Gene Details

Gene
WDR44
Gene Name
WD repeat domain 44
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001184965.1 485 Silent Mutation CAC,CAT H18H NP_001171894.1
NM_001184966.1 485 Silent Mutation CAC,CAT H18H NP_001171895.1
NM_019045.4 485 Silent Mutation CAC,CAT H18H NP_061918.3
XM_011531353.2 485 Silent Mutation CAC,CAT H18H XP_011529655.1
XM_017029600.1 485 UTR 5 XP_016885089.1

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