Product Details

SNP ID

rs200696740

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:83508830 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGCCTGCACCCGGTGCTCCGAGAGC[C/T]CCCGGATCACGGCGAACTGGGCTCG

Phenotype

MIM: 300039

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

POU3F4 PubMed Links

Gene Details

Gene

POU3F4

Gene Name

POU class 3 homeobox 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000307.4	570	Missense Mutation	CCC,CTC	P169L	NP_000298.3

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