Variant #0000000434 (NC_000017.10:del, NM_000267.3:c.(289-1)_(586+1)del (NF1))

Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
DNA change (genomic) (Relative to hg19 / GRCh37) del
Reference -
DB-ID NF1_000015
Frequency -
Average frequency (gnomAD v.2.1.1) Genomic location of variant could not be determined
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2023-10-02 10:52:48 +00:00 (UTC)
Date last edited 2023-10-02 10:53:35 +00:00 (UTC)




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NF1 NM_000267.3 +/+ 4 c.(289-1)_(586+1)del r.? p.?
NF1 NM_001042492.3 +/+ 4 c.(289-1)_(586+1)del r.? p.?