Variant #0000925296 (NC_000011.9:g.108200960C>T, NM_000051.3:c.7327C>T (ATM))

Chromosome 11
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.108200960C>T
DNA change (hg38) -
Published as ATM(NM_000051.3):c.7327C>T (p.Arg2443*)
ISCN -
DB-ID ATM_000271 See all 12 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner VKGL-NL_NKI
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_NKI
Date created 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited 2025-11-01 13:22:20 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ATM NM_000051.3 +/. - c.7327C>T r.(?) p.(Arg2443*)
C11orf65 NM_152587.3 +/. - c.*52788G>A r.(=) p.(=)


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