Variant #0000518192 (NC_000003.11:g.142266585_142266587del, NM_001184.3:c.3339_3341del (ATR))

Chromosome 3
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.142266585_142266587del
DNA change (hg38) g.142547743_142547745del
Published as ATR(NM_001184.3):c.3339_3341del (p.(Ile1114del)), ATR(NM_001184.3):c.3339_3341delCAT (p.I1114del)
ISCN -
DB-ID ATR_000089 See all 2 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ATR NM_001184.3 ?/. - c.3339_3341del r.(?) p.(Ile1114del)


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