Product Details

SNP ID

rs2045066

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.4:1058613 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

ACTCTGAGAAGCCCTGGGTCTTCCA[C/T]ATGAGGGCGTAAATATCCTACATTT

Phenotype

MIM: 612041

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

RNF212 PubMed Links

Gene Details

Gene

RNF212

Gene Name

ring finger protein 212

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001131034.3		Intron			NP_001124506.1
NM_001193318.2		Intron			NP_001180247.1
NM_194439.4		Intron			NP_919420.1
XM_005272274.2		Intron			XP_005272331.1
XM_011513439.1		Intron			XP_011511741.1
XM_011513443.1		Intron			XP_011511745.1
XM_011513444.1		Intron			XP_011511746.1
XM_011513445.2		Intron			XP_011511747.1
XM_011513446.1		Intron			XP_011511748.1
XM_017008039.1		Intron			XP_016863528.1
XM_017008040.1		Intron			XP_016863529.1
XM_017008041.1		Intron			XP_016863530.1
XM_017008042.1		Intron			XP_016863531.1

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