Product Details

SNP ID

rs118152136

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:196508236 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGAGGCTAAGGTTGGAAGACCTCTC[A/G]CCAGGTCTGGCAGCTTCTCAAGCAC

Phenotype

MIM: 612688

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

RNF168 PubMed Links

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	453	Missense Mutation	GCG,GTG	A99V	NP_001071125.1
NM_001320473.1	453	Missense Mutation	GCG,GTG	A91V	NP_001307402.1

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