Variant #0001020666 (NC_000011.9:g.108205832T>C, NM_000051.3:c.8147T>C (ATM))

Chromosome 11
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic (recessive)
DNA change (genomic) (Relative to hg19 / GRCh37) g.108205832T>C
DNA change (hg38) g.108335105T>C
Published as -
ISCN -
DB-ID ATM_000473 See all 36 reported entries
Variant remarks variant associates with milder phenotype (longer survival, later loss of ambulation, fewer telangiectasias, less likely development of cancer, respiratory disease or immunodeficiency)
Reference PubMed: van Os 2019
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 3.0E-5 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2025-01-11 16:06:03 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ATM NM_000051.3 +/. - c.8147T>C r.(?) p.(Val2716Ala)


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