Product Details

SNP ID
rs138007924
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:19914064 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTCCATAAGGCTGTCCAATTCAGGT[C/T]TTCTGTTATCTTTTGAAGTATGTTT
Phenotype
MIM: 613602
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
WDR35 PubMed Links

Gene Details

Gene
WDR35
Gene Name
WD repeat domain 35
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001006657.1 2168 Missense Mutation AAA,AGA K1123R NP_001006658.1
NM_020779.3 2168 Missense Mutation AAA,AGA K1112R NP_065830.2
XM_011533007.2 2168 Missense Mutation AAA,AGA K688R XP_011531309.1

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