Product Details

SNP ID

rs2074496

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.6:31355219 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CGATGGGGACGGTGGACTGGGAAGA[T/C]GGCTCTGGGAAAGGAGGGGAAGATG

Phenotype

MIM: 142830

Polymorphism

T/C, Transition Substitution

Allele Nomenclature

Literature Links

HLA-B PubMed Links

Additional Information

For this assay, SNP(s) [rs70990234] 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

HLA-B

Gene Name

major histocompatibility complex, class I, B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005514.7	987	Silent Mutation	CCA,CCG	P300P	NP_005505.2
XM_011514557.1	987	Intron			XP_011512859.1

Gene

MIR6891

Gene Name

microRNA 6891

There are no transcripts associated with this gene.

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