Variant #0000480219 (NC_000019.9:g.13006872T>C, NM_000159.3:c.572T>C (GCDH))

Chromosome 19
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method ACMG
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.13006872T>C
DNA change (hg38) g.12896058T>C
Published as -
ISCN -
DB-ID GCDH_000014 See all 8 reported entries
Variant remarks ACMG/ACGS: PS4_Moderate, PM3, PP4, PP3_Strong, PS3_Supporting, 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) 8.0E-5 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 2023-12-18 16:59:03 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GCDH NM_000159.3 +/+ 7 c.572T>C r.(?) p.(Met191Thr)


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