Variant #0000550486 (NC_000013.10:g.32918675T>A, NC_000013.10(NM_000059.3):c.6842-20T>A (BRCA2))

Chromosome 13
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.32918675T>A
DNA change (hg38) g.32344538T>A
Published as BRCA2(NM_000059.3):c.6842-20T>A, BRCA2(NM_000059.4):c.6842-20T>A
ISCN -
DB-ID BRCA2_000169 See all 26 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) 0.00024 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +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 -/. - c.6842-20T>A r.(=) p.(=) -


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