Product Details

SNP ID

rs13198255

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.6:136826895 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CAGAGTATATTGGAGCAAGAGCATA[A/G]AATACTGAGTATGAGGCAGAACTTA

Phenotype

MIM: 601757

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

PEX7 PubMed Links

Additional Information

For this assay, SNP(s) [rs77875257] 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

PEX7

Gene Name

peroxisomal biogenesis factor 7

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000288.3		Intron			NP_000279.1
XM_005267019.4		Intron			XP_005267076.1
XM_006715502.1		Intron			XP_006715565.1
XM_017010934.1		Intron			XP_016866423.1

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