Variant #0000953732 (NC_000019.9:g.13008644G>C, NM_000159.3:c.1210G>C (GCDH))

Chromosome 19
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Effect unknown
Classification method ACMG
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.13008644G>C
DNA change (hg38) g.12897830G>C
Published as -
ISCN -
DB-ID GCDH_000328 See all 2 reported entries
Variant remarks ACMG/ACGS: PM3_Supporting, 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) Retrieve
Owner Alexandra Tibelius
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Alexandra Tibelius
Date created 2023-12-18 13:14:24 +01:00 (CET)
Date last edited 2025-01-07 16:02:34 +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.1210G>C r.(?) p.(Ala404Pro)


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