Variant #0001078298 (NC_000017.10:g.41053122T>C, NM_000151.3:c.229T>C (G6PC))

Chromosome 17
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.41053122T>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID G6PC_000068
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs104894566
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-05-28 16:36:01 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
G6PC NM_000151.3 +/. - c.229T>C r.(?) p.(Trp77Arg)


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