Product Details

SNP ID

rs12139104

Assay Type

Functionally tested

NCBI dbSNP Submissions

35

Location

Chr.1:167233907 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ACAGCAATAACATTTATCAAGTCTT[C/T]GTGCCAGTTGTTGTACTAAATGCTT

Phenotype

MIM: 164175

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

POU2F1 PubMed Links

Gene Details

Gene

POU2F1

Gene Name

POU class 2 homeobox 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001198783.1		Intron			NP_001185712.1
NM_001198786.1		Intron			NP_001185715.1
NM_002697.3		Intron			NP_002688.3
XM_011509653.2		Intron			XP_011507955.1
XM_011509654.2		Intron			XP_011507956.1
XM_011509655.1		Intron			XP_011507957.1
XM_017001508.1		Intron			XP_016856997.1

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