Variant #0001042629 (NC_000019.9:g.13006872T>C, NM_000159.3:c.572T>C (GCDH))

Chromosome 19
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.13006872T>C
DNA change (hg38) -
Published as GCDH(NM_000159.3):c.572T>C (p.M191T), GCDH(NM_000159.4):c.572T>C (p.(Met191Thr))
ISCN -
DB-ID GCDH_000014 See all 8 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) 8.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GCDH NM_000159.3 +/. - c.572T>C r.(?) p.(Met191Thr)
SYCE2 NM_001105578.1 +/. - c.*3283A>G r.(=) p.(=)


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