Variant #0000000695 (NC_000017.10:., NC_000017.10(NM_001042492.3):c.5269-1G>C (NF1))

Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
DNA change (genomic) (Relative to hg19 / GRCh37) .
Reference -
DB-ID NF1_000026 See all 2 reported entries
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 2025-10-06 08:51:21 +00:00 (UTC)
Date last edited N/A




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Class     
NF1 NM_001042492.3 +/+ - c.5269-1G>C r.? p.? pathogenic