Variant #0001065519 (NC_000011.9:g.66010747_66010748insTGTCTC, NM_018026.3:c.2888_2889insTGTCTC (PACS1))

Chromosome 11
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.66010747_66010748insTGTCTC
DNA change (hg38) -
Published as PACS1(NM_018026.4):c.2888_2889insTGTCTC (p.(Thr963_*964insValSer))
ISCN -
DB-ID PACS1_000069
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 2026-01-20 18:57:21 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PACS1 NM_018026.3 ?/. - c.2888_2889insTGTCTC r.(?) p.(*964Valext*2)


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