Product Details

SNP ID

rs200595234

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:101540290 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCGGCAGGCCATTGAAGATGAACTT[C/T]GTGAGCACATTGAAAAACTGGAACG

Phenotype

MIM: 607699

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

RNF20 PubMed Links

Gene Details

Gene

RNF20

Gene Name

ring finger protein 20

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_019592.6	586	Missense Mutation	CGT,TGT	R73C	NP_062538.5
XM_011518862.1	586	Missense Mutation	CGT,TGT	R73C	XP_011517164.1

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