Product Details

SNP ID

rs147193465

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:111092380 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTGCAGCTCTGGCAGAGGACTGTTC[C/T]ACTAGACACGCTGAAGGGACTGGGT

Phenotype

MIM: 609669

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

WDR36 PubMed Links

Gene Details

Gene

WDR36

Gene Name

WD repeat domain 36

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_139281.2	209	Missense Mutation	CCA,CTA	P31L	NP_644810.1

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