Variant #0001047229 (NC_000003.11:g.52437748A>C, NM_004656.2:c.1413T>G (BAP1))

Chromosome 3
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.52437748A>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID BAP1_000030 See all 3 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs34736117
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00485 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-08-07 12:29:01 +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     
BAP1 NM_004656.2 -/. - c.1413T>G r.(?) p.(Ala471=)


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