Product Details

SNP ID

rs201722357

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.22:22244966 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACCAGGTTGTGGTCCTCAGCCGGTG[C/G]TGCATCAGCCGCCGGCCATGTCCTC

Phenotype

MIM: 605141

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

VPREB1 PubMed Links

Additional Information

For this assay, SNP(s) [rs9619852] 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

VPREB1

Gene Name

pre-B lymphocyte 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001303509.1	87	Missense Mutation	CTG,GTG	L22V	NP_001290438.1
NM_007128.3	87	Missense Mutation	CTG,GTG	L23V	NP_009059.1

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