Variant #0001038198 (NC_000011.9:g.108236233T>G, NM_000051.3:c.9169T>G (ATM))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.108236233T>G
DNA change (hg38) -
Published as ATM(NM_000051.3):c.9169T>G (p.(Ter3057GlyextTer29))
ISCN -
DB-ID ATM_003663 See all 2 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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
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.9169T>G r.(?) p.(*3057Glyext*29)
C11orf65 NM_152587.3 +?/. - c.*17515A>C r.(=) p.(=)


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