Product Details

SNP ID

rs11867632

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:8396779 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CCCCTCCCTCTGCCTCTCTCGCTTT[C/T]TGAATCCCATTCCATTCCCCATCCT

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

RNF222 PubMed Links

Gene Details

Gene

RNF222

Gene Name

ring finger protein 222

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001146684.2		Intron			NP_001140156.1
XM_011523978.2		Intron			XP_011522280.1
XM_011523979.2		Intron			XP_011522281.1
XM_011523980.2		Intron			XP_011522282.1
XM_011523981.2		Intron			XP_011522283.1

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