Variant #0001046895 (NC_000007.13:g.5754726A>T, NM_207111.3:c.1791T>A (RNF216))

Chromosome 7
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.5754726A>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID RNF216_000043
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs387907369
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-07-10 17:45:01 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RNF216 NM_207111.3 +/. - c.1791T>A r.(?) p.(Cys597Ter)


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