Variant #0000689817 (NC_000006.11:g.87966130_87966132del, NM_015021.1:c.2783_2785del (ZNF292))

Chromosome 6
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.87966130_87966132del
DNA change (hg38) -
Published as ZNF292(NM_015021.2):c.2783_2785delCTC (p.P928del), ZNF292(NM_015021.3):c.2783_2785delCTC (p.P928del)
ISCN -
DB-ID ZNF292_000010 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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZNF292 NM_015021.1 ?/. - c.2783_2785del r.(?) p.(Pro928del)


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