Product Details

SNP ID

rs201791970

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.22:50313678 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTGGGTGAGCTCCAGGAGGTGCCGC[C/T]GCAGCAGGGCGCTCTGCACATCTGA

Phenotype

MIM: 604293

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

DENND6B PubMed Links

Additional Information

For this assay, SNP(s) [rs137921722] 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

DENND6B

Gene Name

DENN domain containing 6B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001001794.3	1322	Missense Mutation			NP_001001794.3
XM_005261914.3	1322	Missense Mutation			XP_005261971.1
XM_011530692.2	1322	Missense Mutation			XP_011528994.1
XM_011530693.2	1322	Missense Mutation			XP_011528995.1
XM_017028801.1	1322	Missense Mutation			XP_016884290.1

Gene

PLXNB2

Gene Name

plexin B2

There are no transcripts associated with this gene.

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