Variant #0001004561 (NC_000019.9:g.20230032_20230036del, NM_007138.1:c.1669_1673del (ZNF90))

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.20230032_20230036del
DNA change (hg38) -
Published as ZNF90(NM_007138.1):c.1669_1673delATAAG (p.(Ile557fs))
ISCN -
DB-ID ZNF90_000002
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 2024-08-28 13:16:32 +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     
ZNF90 NM_007138.1 ?/. - c.1669_1673del r.(?) p.(Ile557Serfs*10)


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