Variant #0000541901 (NC_000011.9:g.108098243A>G, NC_000011.9(NM_000051.3):c.-30-79A>G (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.108098243A>G
DNA change (hg38) g.108227516A>G
Published as ATM(NM_000051.3):c.-30-79A>G
ISCN -
DB-ID ATM_001266
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_NKI
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_NKI
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +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.-30-79A>G r.(=) p.(=)
NPAT NM_002519.2 -/. - c.-4980T>C r.(?) p.(=)


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