Variant #0000259584 (NC_000003.11:g.52440927G>A, NC_000003.11(NM_004656.2):c.581-4C>T (BAP1))

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.52440927G>A
DNA change (hg38) g.52406911G>A
Published as BAP1(NM_004656.3):c.581-4C>T (p.?), BAP1(NM_004656.4):c.581-4C>T
ISCN -
DB-ID BAP1_000012 See all 2 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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-07-07 10:10:56 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BAP1 NM_004656.2 -?/. - c.581-4C>T r.spl? p.?
PHF7 NM_016483.4 -?/. - c.-4406G>A r.(?) p.(=)


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