Variant #0001043243 (NC_000019.9:g.9452565_9452568del, NM_001172651.1:c.-34588_-34585del (ZNF177))

Chromosome 19
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.9452565_9452568del
DNA change (hg38) -
Published as ZNF559(NM_032497.3):c.438_441del (p.(Pro147Thrfs*57))
ISCN -
DB-ID ZNF559_000005
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +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     
ZNF559-ZNF177 NM_001172650.2 ?/. - c.-391+3307_-391+3310del r.(=) p.(=)
ZNF177 NM_001172651.1 ?/. - c.-34588_-34585del r.(?) p.(=)
ZNF559 NM_032497.2 ?/. - c.438_441del r.(?) p.(Pro147Thrfs*57)


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