Variant #0000000432 (NC_000017.10:g.29654761C>G, NM_000267.3:c.5450C>G (NF1))

Chromosome 17
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg19 / GRCh37) g.29654761C>G
Reference -
DB-ID NF1_000013
Frequency -
Average frequency (gnomAD v.2.1.1) 8.0E-5 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 10:46:51 +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 ?/? 37 c.5450C>G r.(?) p.(Ser1817Cys)
NF1 NM_001042492.3 ?/? 38 c.5513C>G r.(?) p.(Ser1838Cys)