Variant #0000520346 (NC_000003.11:g.52440267A>G, NC_000003.11(NM_004656.2):c.783+2T>C (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.52440267A>G
DNA change (hg38) g.52406251A>G
Published as BAP1(NM_004656.2):c.783+2T>C, BAP1(NM_004656.3):c.783+2T>C (p.?)
ISCN -
DB-ID BAP1_000033 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) 0 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +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.783+2T>C r.spl? p.?
PHF7 NM_016483.4 +?/. - c.-5066A>G r.(?) p.(=)


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