Variant #0000323350 (NC_000013.10:g.32972744_32972745insGAATTATAT, NM_000059.3:c.10094_10095insGAATTATAT (BRCA2))

Chromosome 13
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.32972744_32972745insGAATTATAT
DNA change (hg38) g.32398607_32398608insGAATTATAT
Published as BRCA2(NM_000059.3):c.10094_10095insGAATTATAT (p.(Val3365_Ser3366insAsnTyrIle)), BRCA2(NM_000059.4):c.10094_10095insGAATTATAT (p.V3365_S3366insNYI)
ISCN -
DB-ID BRCA2_006065 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) 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-07-07 10:10:56 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
BRCA2 NM_000059.3 ?/. - c.10094_10095insGAATTATAT r.(?) p.(Val3365_Ser3366insAsnTyrIle) -
N4BP2L1 NM_052818.2 ?/. - c.*4335_*4336insTATAATTCA r.(=) p.(=) -


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