Variant #0000804794 (NC_000011.9:g.108175420C>T, NM_000051.3:c.5515C>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.108175420C>T
DNA change (hg38) -
Published as ATM(NM_000051.3):c.5515C>T (p.(Gln1839Ter), p.Q1839*)
ISCN -
DB-ID ATM_000090 See all 7 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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2025-11-01 13:22:20 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ATM NM_000051.3 +/. - c.5515C>T r.(?) p.(Gln1839Ter)
C11orf65 NM_152587.3 +/. - c.*78328G>A r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.