Product Details

SNP ID

rs73213995

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:196469175 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AATTTGAGGCATTCAAGAATGTCCA[C/T]CCTAAAACTGAAAGTGAAATTGCTC

Phenotype

MIM: 612688

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

RNF168 PubMed Links

Gene Details

Gene

RNF168

Gene Name

ring finger protein 168

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_152617.3	4955	UTR 3			NP_689830.2

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