Product Details

SNP ID

rs6774852

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.3:196351556 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ACTTTTAATTAGCCTAGGGATAATA[C/T]GCAATCACGGGGAGAGACTGGAAGC

Phenotype

MIM: 616379

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

UBXN7 PubMed Links

Additional Information

For this assay, SNP(s) [rs115404938] 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

UBXN7

Gene Name

UBX domain protein 7

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_015562.1	6622	Intron			NP_056377.1
XM_011512670.2	6622	UTR 3			XP_011510972.1
XM_011512671.2	6622	UTR 3			XP_011510973.1

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