Variant #0000271829 (NC_000013.10:g.32972922G>A, BRCA2(NM_000059.3):c.*15G>A)

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.32972922G>A
DNA change (hg38) g.32398785G>A
Published as BRCA2(NM_000059.3):c.*15G>A
ISCN -
DB-ID BRCA2_002272 See all 3 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 2.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
BRCA2 NM_000059.3 ?/. - c.*15G>A r.(=) p.(=) -
N4BP2L1 NM_052818.2 ?/. - c.*4157C>T r.(=) p.(=) -