Variant #0000000204 (NC_000011.9:g.108196896C>T, NM_000051.3:c.6919C>T (ATM))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Probably does not affect function
DNA change (genomic) (Relative to hg19 / GRCh37) g.108196896C>T
Reference -
DB-ID ATM_000010
Frequency -
Average frequency (gnomAD v.2.1.1) 0.0014 View details
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2023-06-27 12:32:05 +00:00 (UTC)
Date last edited 2025-10-09 13:29:04 +00:00 (UTC)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Class     
ATM NM_000051.3 -?/-? 47 c.6919C>T r.(?) p.(Leu2307Phe) likely benign