Product Details

SNP ID

rs34856132

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.8:64581136 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGCCGGCGTTGGGGGCGACCCTAGC[A/C]TAAGCAGCCTGCCGGCCGGGGCCGC

Phenotype

MIM: 613483 MIM: 603711

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

BHLHE22 PubMed Links

Additional Information

For this assay, SNP(s) [rs544639534] 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

BHLHE22

Gene Name

basic helix-loop-helix family member e22

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_152414.4	899	Missense Mutation	ATA,CTA	I116L	NP_689627.1

Gene

CYP7B1

Gene Name

cytochrome P450 family 7 subfamily B member 1

There are no transcripts associated with this gene.

Gene

LOC401463

Gene Name

uncharacterized LOC401463

There are no transcripts associated with this gene.

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