Variant #0000930225 (NC_000013.10:g.32914978_32914981del, NM_000059.3:c.6486_6489del (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.32914978_32914981del
DNA change (hg38) -
Published as BRCA2(NM_000059.3):c.6486_6489del (p.(Lys2162AsnfsTer5)), BRCA2(NM_000059.4):c.6486_6489delACAA (p.K2162Nfs*5)
ISCN -
DB-ID BRCA2_000162 See all 42 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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2023-07-07 10:10:56 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
BRCA2 NM_000059.3 +/. - c.6486_6489del r.(?) p.(Lys2162AsnfsTer5) -


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.