Variant #0000953647 (NC_000019.9:g.13002684T>G, NM_000159.3:c.167T>G (GCDH))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Classification method ACMG
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.13002684T>G
DNA change (hg38) g.12891870T>G
Published as -
ISCN -
DB-ID GCDH_000280 See all 2 reported entries
Variant remarks ACMG/ACGS: 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) Retrieve
Owner Sabrina Oeser
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Sabrina Oeser
Date created 2023-12-15 16:10:12 +01:00 (CET)
Date last edited 2024-11-11 13:54:46 +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 +?/+? 4 c.167T>G r.(?) p.(Leu56Arg)


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