Variant #0000622517 (NC_000011.9:g.108175463A>T, NM_000051.3:c.5558A>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.108175463A>T
DNA change (hg38) g.108304736A>T
Published as ATM(NM_000051.3):c.5558A>T (p.D1853V, p.(Asp1853Val), p.Asp1853Val), ATM(NM_000051.4):c.5558A>T (p.D1853V), ATM(NM_001351834.1):c.5558A>T (p.D1853V)
ISCN -
DB-ID ATM_000616 See all 14 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) 0.00496 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-06 12:43:26 +01:00 (CET)
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.5558A>T r.(?) p.(Asp1853Val)
C11orf65 NM_152587.3 -?/. - c.*78285T>A r.(=) p.(=)


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