Variant #0000000348 (NC_000008.10:g.90993017T>C, NM_002485.4:c.425A>G (NBN))

Chromosome 8
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Does not affect function
DNA change (genomic) (Relative to hg19 / GRCh37) g.90993017T>C
Reference -
DB-ID NBN_000002
Frequency -
Average frequency (gnomAD v.2.1.1) 0.00017 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 13:36:33 +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.425A>G r.(?) p.(Asn142Ser)