Variant #0000863370 (NC_000013.10:g.32972760G>A, NM_000059.3:c.10110G>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.32972760G>A
DNA change (hg38) -
Published as BRCA2(NM_000059.3):c.10110G>A (p.R3370=, p.(Arg3370=)), BRCA2(NM_000059.4):c.10110G>A (p.R3370=)
ISCN -
DB-ID BRCA2_000483 See all 29 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) 0.0014 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2022-05-09 15:51:19 +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.10110G>A r.(?) p.(Arg3370=) -
N4BP2L1 NM_052818.2 -/. - c.*4319C>T r.(=) p.(=) -


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