Variant #0001039837 (NC_000014.8:g.105685327G>A, NM_001100913.2:c.-95929G>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.105685327G>A
DNA change (hg38) -
Published as BRF1(NM_001519.4):c.1515+8C>T
ISCN -
DB-ID BRF1_000053
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) 1.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +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.-95929G>A r.(?) p.(=)
BRF1 NM_001242786.1 -?/. - c.1236+8C>T r.(=) p.(=)
BTBD6 NM_033271.2 -?/. - c.-29660G>A r.(?) p.(=)


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