Variant #0000853731 (NC_000014.8:g.105821439G>A, NM_001100913.2:c.348G>A (PACS2))

Chromosome 14
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.105821439G>A
DNA change (hg38) -
Published as PACS2(NM_001100913.3):c.348G>A (p.Q116=)
ISCN -
DB-ID BRF1_000026
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) 0.00075 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-05-09 15:40:45 +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.348G>A r.(?) p.(Gln116=)
BRF1 NM_001242786.1 -?/. - c.-39942C>T r.(?) p.(=)


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