Variant #0000011759 (NC_000011.10:g.108121753_108121754del, ATM(NM_000051.4):c.1564_1565del)

Chromosome 11
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
DNA change (genomic) (Relative to hg38 / GRCh38) g.108121753_108121754del
Reference -
DB-ID ATM_000208 See all 4 reported entries
dbSNP ID rs1374409941
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Guillermo Alberto-Instituto Fleming
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Instituto Nacional del Cancer
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Protein     

Zygosity     

Co_ocurrence     

RNA change     

Review status     
ATM NM_000051.4 +/+ 10 c.1564_1565del p.(Glu522Ilefs*43) Hetero no r.(?) -