Variant #0000929250 (NC_000006.11:g.87953322T>G, NM_015021.1:c.871T>G (ZNF292))

Chromosome 6
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.87953322T>G
DNA change (hg38) -
Published as ZNF292(NM_015021.1):c.871T>G (p.(Cys291Gly)), ZNF292(NM_015021.3):c.871T>G (p.C291G)
ISCN -
DB-ID ZNF292_000020 See all 2 reported entries
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) 0.00101 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-07-07 10:10:56 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZNF292 NM_015021.1 -?/. - c.871T>G r.(?) p.(Cys291Gly)


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