Variant #0000566896 (NC_000019.9:g.35249942_35249943dup, NM_001007248.2:c.1764_1765dup (ZNF599))

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.35249942_35249943dup
DNA change (hg38) g.34759037_34759038dup
Published as ZNF599(NM_001007248.2):c.1765_1766insTT (p.(Ter589Phe))
ISCN -
DB-ID ZNF599_000001
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZNF599 NM_001007248.2 ?/. - c.1764_1765dup r.(?) p.(Ter589PheextTer14)


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