Variant #0001024844 (NC_000003.11:g.52441235G>A, NM_004656.2:c.535C>T (BAP1))

Chromosome 3
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.52441235G>A
DNA change (hg38) -
Published as BAP1(NM_004656.2):c.535C>T (p.R179W), BAP1(NM_004656.3):c.535C>T (p.(Arg179Trp)), BAP1(NM_004656.4):c.535C>T (p.R179W)
ISCN -
DB-ID BAP1_000013 See all 5 reported entries
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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     
BAP1 NM_004656.2 +?/. - c.535C>T r.(?) p.(Arg179Trp)
PHF7 NM_016483.4 +?/. - c.-4098G>A r.(?) p.(=)


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