Variant #0001024849 (NC_000003.11:g.52724613G>A, NM_018313.4:c.-4861C>T (PBRM1))

Chromosome 3
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.52724613G>A
DNA change (hg38) -
Published as GNL3(NM_014366.5):c.547G>A (p.V183I)
ISCN -
DB-ID GNL3_000004
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2025-02-07 18:57:27 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SPCS1 NM_014041.3 ?/. - c.-15449G>A r.(?) p.(=)
GNL3 NM_014366.4 ?/. - c.547G>A r.(?) p.(Val183Ile)
PBRM1 NM_018313.4 ?/. - c.-4861C>T r.(?) p.(=)
GLT8D1 NM_152932.2 ?/. - c.*4248C>T r.(=) p.(=)


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