Product Details

SNP ID

rs199903182

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:202884467 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TATGGTCCCAAGATGCACTGCAGAT[C/T]TCTTCAGCATCTGACCACAGAACTG

Phenotype

MIM: 616620

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

WDR12 PubMed Links

Gene Details

Gene

WDR12

Gene Name

WD repeat domain 12

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_018256.3	1437	Silent Mutation	GAA,GAG	E270E	NP_060726.3
XM_011511469.2	1437	Silent Mutation	GAA,GAG	E132E	XP_011509771.1

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