Product Details

SNP ID
rs882856
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.11:120236702 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GAGTCTCCAAGAACTGCTAAAGGAG[A/G]AAGGGGTAAAGGAGTTCTCTACGTT
Phenotype
MIM: 607394
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
OAF PubMed Links

Gene Details

Gene
OAF
Gene Name
out at first homolog
There are no transcripts associated with this gene.

Gene
POU2F3
Gene Name
POU class 2 homeobox 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001244682.1 63 Missense Mutation GAA,GGA E10G NP_001231611.1
NM_014352.3 63 Intron NP_055167.2
XM_011542739.2 63 Intron XP_011541041.1
XM_011542740.2 63 Intron XP_011541042.1
XM_011542741.2 63 Intron XP_011541043.1
XM_011542742.2 63 Intron XP_011541044.1
XM_011542743.2 63 Intron XP_011541045.1
XM_017017487.1 63 Intron XP_016872976.1

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