Variant #0000307181 (NC_000007.13:g.5662506C>T, NM_207111.3:c.2757G>A (RNF216))

Chromosome 7
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.5662506C>T
DNA change (hg38) g.5622875C>T
Published as RNF216(NM_207111.3):c.2757G>A (p.P919=), RNF216(NM_207111.4):c.2757G>A (p.P919=)
ISCN -
DB-ID RNF216_000002 See all 2 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00033 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RNF216 NM_207111.3 -?/. - c.2757G>A r.(?) p.(Pro919=)


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