Variant #0000480244 (NC_000019.9:g.13008578G>A, NM_000159.3:c.1144G>A (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.13008578G>A
DNA change (hg38) g.12897764G>A
Published as -
ISCN -
DB-ID GCDH_000039 See all 5 reported entries
Variant remarks ACMG/ACGS: PS4_Moderate, PM3_Supporting, 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) 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 2024-12-04 18:16:05 +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 +/+? 11 c.1144G>A r.(?) p.(Ala382Thr)


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