Variant #0000953644 (NC_000019.9:g.13002214G>A, NC_000019.9(NM_000159.3):c.91+5G>A (GCDH))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Affects function
Classification method ACMG
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.13002214G>A
DNA change (hg38) g.12891400G>A
Published as IVS1+5G>A
ISCN -
DB-ID GCDH_000277 See all 7 reported entries
Variant remarks ACMG/ACGS: PS1, PS4_Moderate, PM3, PP3, 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 Sabrina Oeser
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Sabrina Oeser
Date created 2023-12-15 15:56:29 +01:00 (CET)
Date last edited 2024-11-08 13:43:06 +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 +?/+ 2i c.91+5G>A r.spl? p.?


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