Variant #0000036396 (NC_000019.9:g.13002736del, NM_000159.3:c.219del (GCDH))

Chromosome 19
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification pathogenic (recessive)
DNA change (genomic) (Relative to hg19 / GRCh37) g.13002736del
DNA change (hg38) g.12891922del
Published as c.219delC
ISCN -
DB-ID GCDH_000066 See all 10 reported entries
Variant remarks Geographic origin: Germany
Reference PubMed: Zschocke 2000
ClinVar ID -
dbSNP ID -
Origin Germline/De novo (untested)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Svenja Wagner
Database submission license No license selected
Created by Svenja Wagner
Date created 2014-05-13 12:24:41 +02:00 (CEST)
Date last edited 2024-11-11 14:52:25 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GCDH NM_000159.3 +/+ 4 c.219del r.(?) p.(Tyr74Thrfs*68)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.