Variant #0000000350 (NC_000008.10:g.90967646A>G, NM_002485.4:c.1262T>C (NBN))

Chromosome 8
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg19 / GRCh37) g.90967646A>G
Reference -
DB-ID NBN_000004
Frequency -
Average frequency (gnomAD v.2.1.1) 0.00038 View details
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2023-07-17 13:37:28 +00:00 (UTC)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NBN NM_002485.4 ?/? - c.1262T>C r.(?) p.(Leu421Ser)