Variant #0000893951 (NC_000017.10:g.42153393G>A, NM_138387.3:c.1023G>A (G6PC3))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.42153393G>A
DNA change (hg38) -
Published as G6PC3(NM_138387.3):c.1023G>A (p.P341=)
ISCN -
DB-ID G6PC3_000016
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) 5.0E-5 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:41:49 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HDAC5 NM_001015053.1 -?/. - c.*2351C>T r.(=) p.(=)
G6PC3 NM_138387.3 -?/. - c.1023G>A r.(?) p.(Pro341=)


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