Variant #0000889580 (NC_000011.9:g.108236070C>T, NM_000051.3:c.9006C>T (ATM))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.108236070C>T
DNA change (hg38) -
Published as ATM(NM_000051.3):c.9006C>T (p.(=), p.F3002=), ATM(NM_000051.4):c.9006C>T (p.F3002=)
ISCN -
DB-ID ATM_003299 See all 3 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) 0.00032 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited 2025-02-07 18:57:27 +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.9006C>T r.(?) p.(Phe3002=)
C11orf65 NM_152587.3 -?/. - c.*17678G>A r.(=) p.(=)


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