Product Details

SNP ID

rs195860

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:98835500 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGGGCGCCGGCGGGCAGCCGGCCGG[G/T]CTGCACCACCACGGCCTGCGGGACG

Phenotype

MIM: 600494

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

POU3F2 PubMed Links

Gene Details

Gene

POU3F2

Gene Name

POU class 3 homeobox 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005604.3	797	Silent Mutation	GGG,GGT	G209G	NP_005595.2

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