Variant #0000000683 (NC_000017.10:g.29553526dup, NM_000267.3:c.2075dup (NF1))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.29553526dup
Reference -
DB-ID NF1_000024
Frequency -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2025-10-06 07:56:39 +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     
NF1 NM_000267.3 +?/+? - c.2075dup r.? p.Tyr692Ter likely pathogenic
NF1 NM_001042492.3 +?/+? - c.2075dup r.? p.Tyr692Ter likely pathogenic