Product Details

SNP ID

rs10876043

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.12:50510361 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AAAATTAATCTTGTTTGACAGCCCC[A/G]TGGCATTGAGCTGGATTTTTGAATA

Phenotype

MIM: 611379

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

DIP2B PubMed Links

Additional Information

For this assay, SNP(s) [rs79799217] are located under a primer 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

DIP2B

Gene Name

disco interacting protein 2 homolog B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_173602.2		Intron			NP_775873.2
XM_005269044.1		Intron			XP_005269101.1
XM_006719520.3		Intron			XP_006719583.1
XM_006719521.3		Intron			XP_006719584.1
XM_011538594.2		Intron			XP_011536896.1
XM_011538595.2		Intron			XP_011536897.1
XM_011538596.2		Intron			XP_011536898.1
XM_017019699.1		Intron			XP_016875188.1
XM_017019700.1		Intron			XP_016875189.1
XM_017019701.1		Intron			XP_016875190.1
XM_017019702.1		Intron			XP_016875191.1
XM_017019703.1		Intron			XP_016875192.1
XM_017019704.1		Intron			XP_016875193.1
XM_017019705.1		Intron			XP_016875194.1

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