Variant #0000626532 (NC_000002.11:g.96781203_96781214delinsCTGCCAAAC, NM_000682.5:c.675_686delinsGTTTGGCAG (ADRA2B))

Chromosome 2
Allele Parent #1
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.96781203_96781214delinsCTGCCAAAC
DNA change (hg38) g.96115464_96115475delinsCTGCCAAAC
Published as 675_686delTGGTGGGGCTTTinsGTTTGGCAG
ISCN -
DB-ID ADRA2B_000005 See all 3 reported entries
Variant remarks variant initially linked to ADCME phenotype
Reference PubMed: Corbett 2019
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2019-12-19 14:02:00 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ADRA2B NM_000682.5 ?/. - c.675_686delinsGTTTGGCAG r.(?) p.(His225_Leu229delinsGlnPheGlyArg)


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