Variant #0000953645 (NC_000019.9:g.13002337G>T, NC_000019.9(NM_000159.3):c.127+1G>T (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.13002337G>T
DNA change (hg38) g.12891523G>T
Published as -
ISCN -
DB-ID GCDH_000278 See all 2 reported entries
Variant remarks ACMG/ACGS: PM3_Supporting, PVS1_Moderate, 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 16:03:17 +01:00 (CET)
Date last edited 2024-11-08 15:29:09 +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 +/? 3i c.127+1G>T r.spl? p.?


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