Product Details

SNP ID

rs12126822

Assay Type

Functionally tested

NCBI dbSNP Submissions

17

Location

Chr.1:185066848 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGGTGGGGGCAGGGGTAGTAGTAGT[C/G]TTAGAGGAGATGAGATAGTGATTGA

Phenotype

MIM: 608985

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

RNF2 PubMed Links

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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