Variant #0000656668 (NC_000011.9:g.108224615A>C, NC_000011.9(NM_000051.3):c.8786+8A>C (ATM))

Chromosome 11
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.108224615A>C
DNA change (hg38) g.108353888A>C
Published as ATM(NM_000051.3):c.8786+8A>C (p.(=)), ATM(NM_001351834.1):c.8786+8A>C
ISCN -
DB-ID ATM_000627 See all 11 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) 0.02607 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 2020-03-23 16:13:27 +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.8786+8A>C r.(=) p.(=)
C11orf65 NM_152587.3 -/. - c.*29133T>G r.(=) p.(=)


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