Product Details

SNP ID

rs4916497

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.3:196471662 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

TACCGCTGAGCTGTGCAGAAGCTCA[C/T]GTGTCTATGCAGTCCTTACAATCAC

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	2468	UTR 3			NP_689830.2

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