Variant #0000874091 (NC_000013.10:g.32893467G>C, NC_000013.10(NM_000059.3):c.316+5G>C (BRCA2))

Chromosome 13
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.32893467G>C
DNA change (hg38) -
Published as c.316+5G>C
ISCN -
DB-ID BRCA2_000015 See all 3 reported entries
Variant remarks classification based on multiple evidence types incl. bioinformatics, RNA analysis, mini-gene splicing assays, clinical data, etc.
Reference PubMed: Thomassen 2022
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Maaike Vreeswijk
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Maaike Vreeswijk
Date created 2022-08-04 13:09:51 +02:00 (CEST)
Date last edited 2022-11-15 18:03:57 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
BRCA2 NM_000059.3 +/. 3i c.316+5G>C r.? p.? -


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