Variant #0001005177 (NC_000019.9:g.58189689C>A, NM_138347.4:c.-3843C>A (ZNF551))

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.58189689C>A
DNA change (hg38) -
Published as ZSCAN4(NM_152677.2):c.718C>A (p.(Pro240Thr))
ISCN -
DB-ID ZNF551_000004
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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZNF551 NM_138347.4 ?/. - c.-3843C>A r.(?) p.(=)
ZSCAN4 NM_152677.2 ?/. - c.718C>A r.(?) p.(Pro240Thr)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.