Product Details

SNP ID

rs10883931

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.10:103864197 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TGCTGGAGGTCAGGACAGTGGTTGC[C/T]TCTGAGAGGTATGAGCTAGGAGGGG

Phenotype

MIM: 613128

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

OBFC1 PubMed Links

Additional Information

For this assay, SNP(s) [rs10883932] are located under a probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

OBFC1

Gene Name

oligonucleotide/oligosaccharide binding fold containing 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_024928.4		Intron			NP_079204.2
XM_006717976.3		Intron			XP_006718039.1
XM_011540184.2		Intron			XP_011538486.1
XM_017016669.1		Intron			XP_016872158.1
XM_017016670.1		Intron			XP_016872159.1

Gene

SH3PXD2A

Gene Name

SH3 and PX domains 2A

There are no transcripts associated with this gene.

View Full Product Details