Product Details

SNP ID

rs3766721

Assay Type

Functionally Tested

NCBI dbSNP Submissions

2

Location

Chr.1:185054240 on Build GRCh38

Set Membership

JSNP

Context Sequence [VIC/FAM]

TATGCCTTGGACTAAACTGGACATT[A/G]TCATTCATTCTTTTTGCTAATCTGA

Phenotype

MIM: 608985

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

RNF2 PubMed Links

Additional Information

For this assay, SNP(s) [rs113970151] 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

RNF2

Gene Name

ring finger protein 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_007212.3		Intron			NP_009143.1
XM_005245413.3		Intron			XP_005245470.1
XM_011509851.2		Intron			XP_011508153.1
XM_011509852.2		Intron			XP_011508154.1

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