Product Details

SNP ID
rs141164229
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:135186312 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTCTCCAGAACCTTCTCATCGCCAC[C/T]CAGCTGCAAGAGGACAGGAAAGAGG
Phenotype
MIM: 616303
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
WDR91 PubMed Links

Gene Details

Gene
WDR91
Gene Name
WD repeat domain 91
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_014149.3 1685 Missense Mutation AGT,GGT S695G NP_054868.3
XM_011516083.2 1685 Missense Mutation AGT,GGT S740G XP_011514385.1
XM_011516086.2 1685 Missense Mutation AGT,GGT S714G XP_011514388.1
XM_017012070.1 1685 Missense Mutation AGT,GGT S721G XP_016867559.1
XM_017012071.1 1685 Missense Mutation AGT,GGT S497G XP_016867560.1
XM_017012072.1 1685 Missense Mutation AGT,GGT S452G XP_016867561.1

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