Variant #0000480211 (NC_000019.9:g.13007231T>C, NM_000159.3:c.848T>C (GCDH))

Chromosome 19
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Probably affects function
Classification method ACMG
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.13007231T>C
DNA change (hg38) g.12896417T>C
Published as -
ISCN -
DB-ID GCDH_000004 See all 4 reported entries
Variant remarks ACMG/ACGS: PS4_Supporting, PM3_Supporting, PP3_Strong, PM2_Supporting (December 2023)
Reference -
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner Isabelle Rinke
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2019-05-22 09:22:27 +02:00 (CEST)
Date last edited 2024-11-29 15:54:29 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GCDH NM_000159.3 +/+? 8 c.848T>C r.848u>c p.Leu283Pro


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