Variant #0001000764 (NC_000014.8:g.105818794_105818796del, NM_001100913.2:c.287_289del (PACS2))

Chromosome 14
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.105818794_105818796del
DNA change (hg38) -
Published as PACS2(NM_001100913.2):c.287_289delTCT (p.(Phe96del))
ISCN -
DB-ID BRF1_000043
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     
PACS2 NM_001100913.2 ?/. - c.287_289del r.(?) p.(Phe96del)
BRF1 NM_001242786.1 ?/. - c.-37297_-37295del r.(?) p.(=)


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