Product Details

SNP ID
rs142589253
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.9:113316876 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACCAACAGCCAGAGAAGTCAAGGGT[C/G]CTGATCCATCCAGAGACAAGGTGAA
Phenotype
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
WDR31 PubMed Links

Gene Details

Gene
WDR31
Gene Name
WD repeat domain 31
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001006615.2 1193 Missense Mutation GCA,GGA A201G NP_001006616.1
NM_001012361.3 1193 Missense Mutation GCA,GGA A326G NP_001012361.1
NM_145241.4 1193 Missense Mutation GCA,GGA A325G NP_660284.1
XM_011518194.2 1193 Missense Mutation GCA,GGA A301G XP_011516496.1

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