Variant #0000000438 (NC_000017.10:g.29527461C>T, NM_000267.3:c.910C>T (NF1))

Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.29527461C>T
Reference -
DB-ID NF1_000018
Frequency -
Average frequency (gnomAD v.2.1.1) 0 View details
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 11:09:32 +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     
NF1 NM_000267.3 +/+ 9 c.910C>T r.(?) p.(Arg304Ter)
NF1 NM_001042492.3 +/+ 9 c.910C>T r.(?) p.(Arg304Ter)