Product Details

SNP ID
rs140529940
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.9:134139910 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CGGAGGAGAAGAAGCCCGAGACCGA[G/T]GCCGCCAGAGCACAGCCAACCCCTT
Phenotype
MIM: 609012
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
WDR5 PubMed Links

Gene Details

Gene
WDR5
Gene Name
WD repeat domain 5
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_017588.2 119 Missense Mutation GAG,GAT E11D NP_060058.1
NM_052821.3 119 Missense Mutation GAG,GAT E11D NP_438172.1
XM_005272163.1 119 Missense Mutation GAG,GAT E11D XP_005272220.1

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