Variant #0001016486 (NC_000011.9:g.108216597G>C, NM_000051.3:c.8546G>C (ATM))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.108216597G>C
DNA change (hg38) g.108345870G>C
Published as -
ISCN -
DB-ID ATM_000108 See all 4 reported entries
Variant remarks ACMG PS3_mod, PM2_sup, PM3_mod, PP3_sup
Reference PubMed: Richardson 2024, Journal: Richardson 2024
ClinVar ID ClinVar-490737
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2024-11-05 11:28:57 +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.8546G>C r.(=) p.(Arg2849Pro)


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