Variant #0000913483 (NC_000011.9:g.108235872C>T, NM_000051.3:c.8914C>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.108235872C>T
DNA change (hg38) -
Published as ATM(NM_000051.3):c.8914C>T (p.Q2972*)
ISCN -
DB-ID ATM_003345
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-01-11 15:44:22 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ATM NM_000051.3 +/. - c.8914C>T r.(?) p.(Gln2972*)
C11orf65 NM_152587.3 +/. - c.*17876G>A r.(=) p.(=)


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