Variant #0000000592 (NC_000008.10:g.30921954G>C, NC_000008.10(NM_000553.4):c.355+4G>C (WRN))

Chromosome 8
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Probably does not affect function
DNA change (genomic) (Relative to hg19 / GRCh37) g.30921954G>C
Reference -
DB-ID WRN_000001
Frequency -
Average frequency (gnomAD v.2.1.1) 0.00155 View details
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2024-06-03 15:55:36 +00:00 (UTC)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Class     
WRN NM_000553.4 -?/-? - c.355+4G>C r.spl? p.? -