Variant #0000269313 (NC_000013.10:g.32972280G>A, NC_000013.10(NM_000059.3):c.9649-19G>A (BRCA2))

Chromosome 13
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Does not affect function
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.32972280G>A
DNA change (hg38) g.32398143G>A
Published as BRCA2(NM_000059.3):c.9649-19G>A (p.(=)), BRCA2(NM_000059.4):c.9649-19G>A
ISCN -
DB-ID BRCA2_001513 See all 23 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) 0.00131 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
BRCA2 NM_000059.3 -?/- - c.9649-19G>A r.(=) p.(=) -
N4BP2L1 NM_052818.2 -?/- - c.*4799C>T r.(=) p.(=) -


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