Product Details

SNP ID

rs739830

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.17:19411298 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GATACCATCCCCCGACCTCACCTTC[C/T]ACCTACCGCAGCCTGCTAGCCTTTC

Phenotype

MIM: 601237

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

RNF112 PubMed Links

Additional Information

For this assay, SNP(s) [rs77802805] are located under a primer 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

RNF112

Gene Name

ring finger protein 112

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_007148.4	4130	UTR 5			NP_009079.2
XM_006721571.3	4130	UTR 5			XP_006721634.1
XM_006721572.3	4130	UTR 5			XP_006721635.1
XM_006721573.3	4130	Intron			XP_006721636.1

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