Variant #0001015118 (NC_000014.8:g.105814830G>A, NM_001100913.2:c.120G>A (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.105814830G>A
DNA change (hg38) -
Published as PACS2(NM_001100913.3):c.120G>A (p.R40=)
ISCN -
DB-ID BRF1_000050
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) 0 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-10-29 21:08:56 +01:00 (CET)
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.120G>A r.(?) p.(=)
BRF1 NM_001242786.1 ?/. - c.-33333C>T r.(?) p.(=)


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