Product Details

SNP ID

rs199641376

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.3:196509529 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTCAATTGATACTCACTGGAGTGCC[C/T]GAACTGCTGTCCACATCTCATCTTG

Phenotype

MIM: 612688

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

RNF168 PubMed Links

Additional Information

For this assay, SNP(s) [rs11926701] 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

RNF168

Gene Name

ring finger protein 168

There are no transcripts associated with this gene.

Gene

SMCO1

Gene Name

single-pass membrane protein with coiled-coil domains 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001077657.2	348	Missense Mutation			NP_001071125.1
NM_001320473.1	348	Missense Mutation			NP_001307402.1

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