Product Details

SNP ID
rs190070503
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:19914145 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTGCTGTTTCTGTTCTGAACTGAGG[G/T]TCTCTAAAGATTTAAGTTTAATGAA
Phenotype
MIM: 613602
Polymorphism
G/T, Transversion 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 2087 Missense Mutation AAC,ACC N1096T NP_001006658.1
NM_020779.3 2087 Missense Mutation AAC,ACC N1085T NP_065830.2
XM_011533007.2 2087 Missense Mutation AAC,ACC N661T XP_011531309.1

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