Product Details

SNP ID
rs149236275
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:19914077 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCCAATTCAGGTTTTCTGTTATCTT[C/T]TGAAGTATGTTTGGTGAAGATTTCT
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 2155 Missense Mutation AAA,GAA K1119E NP_001006658.1
NM_020779.3 2155 Missense Mutation AAA,GAA K1108E NP_065830.2
XM_011533007.2 2155 Missense Mutation AAA,GAA K684E XP_011531309.1

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