Variant #0000000087 (NC_000017.10:g.29509520A>C, NC_000017.10(NM_000267.3):c.731-6A>C (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.29509520A>C
Reference -
DB-ID NF1_000005
Frequency -
Average frequency (gnomAD v.2.1.1) 0.00033 View details
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2020-03-03 13:05:59 +00:00 (UTC)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NF1 NM_000267.3 ?/? 8 c.731-6A>C r.(=) p.(=)