Variant #0001049125 (NC_000003.11:g.52637885C>T, NC_000003.11(NM_018313.4):c.2568-137G>A (PBRM1))

Chromosome 3
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.52637885C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID PBRM1_000018
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1176875788
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 2025-10-10 20:55:01 +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.2568-137G>A r.(?) p.(?)


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