Variant #0000931003 (NC_000019.9:g.13008632G>A, NM_000159.3:c.1198G>A (GCDH))

Chromosome 19
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.13008632G>A
DNA change (hg38) g.12897818G>A
Published as GCDH(NM_000159.4):c.1198G>A (p.V400M)
ISCN -
DB-ID GCDH_000017 See all 35 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.0001 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2023-07-07 10:10:56 +02:00 (CEST)
Date last edited 2025-02-07 18:57:27 +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.1198G>A r.(?) p.(Val400Met)
SYCE2 NM_001105578.1 +/+ - c.*1523C>T r.(=) p.(=)


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