Variant #0001047234 (NC_000003.11:g.52668638G>A, NM_018313.4:c.1281C>T (PBRM1))

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.52668638G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID PBRM1_000013
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs17052357
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.04128 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-08-07 15:08:01 +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     
PBRM1 NM_018313.4 -/. - c.1281C>T r.(?) p.(Pro427=)


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