Variant #0000503517 (NC_000001.10:g.154569366_154569367insT, NM_001111.4:c.2184_2185insA (ADAR))

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.154569366_154569367insT
DNA change (hg38) g.154596890_154596891insT
Published as ADAR(NM_001193495.2):c.1299_1300insA (p.G434Rfs*15)
ISCN -
DB-ID ADAR_000061
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 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ADAR NM_001111.4 +/. - c.2184_2185insA r.(?) p.(Gly729ArgfsTer15)


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