Variant #0000691602 (NC_000014.8:g.105695164G>C, NM_001100913.2:c.-86092G>C (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.105695164G>C
DNA change (hg38) -
Published as BRF1(NM_001519.4):c.781C>G (p.R261G)
ISCN -
DB-ID BRF1_000022
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +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.-86092G>C r.(?) p.(=)
BRF1 NM_001242786.1 ?/. - c.436C>G r.(?) p.(Arg146Gly)
BTBD6 NM_033271.2 ?/. - c.-19823G>C r.(?) p.(=)


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