Variant #0000520350 (NC_000003.11:g.52441269C>T, NM_004656.2:c.501G>A (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.52441269C>T
DNA change (hg38) g.52407253C>T
Published as BAP1(NM_004656.2):c.501G>A (p.A167=)
ISCN -
DB-ID BAP1_000037
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) 0.00069 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 2020-06-15 10:52:49 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BAP1 NM_004656.2 -?/. - c.501G>A r.(?) p.(Ala167=)
PHF7 NM_016483.4 -?/. - c.-4064C>T r.(?) p.(=)


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