Variant #0000852660 (NC_000011.9:g.108098321G>T, NC_000011.9(NM_000051.3):c.-30-1G>T (ATM))

Chromosome 11
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.108098321G>T
DNA change (hg38) -
Published as ATM(NM_001351834.1):c.-30-1G>T
ISCN -
DB-ID ATM_003150
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:40:45 +02:00 (CEST)
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.-30-1G>T r.spl? p.?
NPAT NM_002519.2 ?/. - c.-5058C>A r.(?) p.(=)


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