Variant #0001017878 (NC_000019.9:g.13007757G>A, NM_000159.3:c.886G>A (GCDH))

Chromosome 19
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Probably does not affect function
Classification method ACMG
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.13007757G>A
DNA change (hg38) g.12896943G>A
Published as -
ISCN -
DB-ID GCDH_000186 See all 3 reported entries
Variant remarks ACMG/ACGS: PP3_Strong, BS1, BP5 (December 2024)
Reference -
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00049 View details
Owner Alexandra Tibelius
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Alexandra Tibelius
Date created 2024-12-03 12:37:53 +01:00 (CET)
Date last edited 2024-12-03 12:38:53 +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 ?/-? 9 c.886G>A r.(?) p.(Gly296Ser)


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