Variant #0000345365 (NC_000013.10:g.32972834del, NM_000059.3:c.10184del (BRCA2))

Chromosome 13
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.32972834del
DNA change (hg38) g.32398697del
Published as BRCA2(NM_000059.3):c.10184delA (p.E3395Gfs*32), BRCA2(NM_000059.4):c.10184delA (p.E3395Gfs*32)
ISCN -
DB-ID BRCA2_001340 See all 27 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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
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     

Haplotype     
BRCA2 NM_000059.3 -?/. - c.10184del r.(?) p.(Glu3395GlyfsTer32) -
N4BP2L1 NM_052818.2 -?/. - c.*4245del r.(?) p.(=) -


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