Variant #0000271937 (NC_000013.10:g.32913565dup, NM_000059.3:c.5073dup (BRCA2))

Chromosome 13
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.32913565dup
DNA change (hg38) g.32339428dup
Published as BRCA2(NM_000059.3):c.5073dupA (p.Trp1692Metfs*3), BRCA2(NM_000059.3):c.5073dupA (p.W1692Mfs*3)
ISCN -
DB-ID BRCA2_001899 See all 44 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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-11-01 13:22:20 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
BRCA2 NM_000059.3 +/. - c.5073dup r.(?) p.(Trp1692MetfsTer3) -


Screenscraping/webscraping (interacting with LOVD using scripts to download data) is strictly prohibited.
Use our APIs to retrieve data.