Variant #0000980796 (NC_000014.8:g.105693016dup, NM_001100913.2:c.-88240dup (PACS2))

Chromosome 14
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.105693016dup
DNA change (hg38) -
Published as BRF1(NM_001519.4):c.876dup (p.(Ser293LeufsTer15))
ISCN -
DB-ID BRF1_000036
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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PACS2 NM_001100913.2 +/. - c.-88240dup r.(?) p.(=)
BRF1 NM_001242786.1 +/. - c.531dup r.(?) p.(Ser178Leufs*15)
BTBD6 NM_033271.2 +/. - c.-21971dup r.(?) p.(=)


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