Product Details

SNP ID

rs150150229

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:146639970 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGCAAGAGCCACCACCACCATCCAC[C/T]CCACCACAGCCCCTTCAAACCGGAC

Phenotype

MIM: 113725

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

POU4F2 PubMed Links

Gene Details

Gene

POU4F2

Gene Name

POU class 4 homeobox 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004575.2	640	Missense Mutation	CCC,CTC	P131L	NP_004566.2

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