Variant #0001047057 (NC_000003.11:g.52438566G>A, NM_004656.2:c.1153C>T (BAP1))

Chromosome 3
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.52438566G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID BAP1_000084
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1553645164
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-08-04 10:41:01 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BAP1 NM_004656.2 +/. - c.1153C>T r.(?) p.(Arg385Ter)


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