Variant #0000852722 (NC_000011.9:g.108196143C>T, NM_000051.3:c.6679C>T (ATM))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.108196143C>T
DNA change (hg38) -
Published as ATM(NM_000051.3):c.6679C>T (p.R2227C), ATM(NM_001351834.2):c.6679C>T (p.R2227C)
ISCN -
DB-ID ATM_000256 See all 24 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) 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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ATM NM_000051.3 +?/. - c.6679C>T r.(?) p.(Arg2227Cys)
C11orf65 NM_152587.3 +?/. - c.*57605G>A r.(=) p.(=)


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