Variant #0000480428 (NC_000019.9:g.13008567C>T, NM_000159.3:c.1133C>T (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.13008567C>T
DNA change (hg38) g.12897753C>T
Published as -
ISCN -
DB-ID GCDH_000251 See all 4 reported entries
Variant remarks ACMG/ACGS: PM5_Supporting, PS4_Supporting, PM3, PP3_Moderate, PM2_Supporting (December 2024)
Reference -
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
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 2025-01-10 14:18:33 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GCDH NM_000159.3 +/+? 11 c.1133C>T r.(?) p.(Ala378Val)


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