Variant #0000272043 (NC_000013.10:g.32929416_32929418del, NM_000059.3:c.7426_7428del (BRCA2))

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.32929416_32929418del
DNA change (hg38) g.32355279_32355281del
Published as BRCA2(NM_000059.3):c.7426_7428delGAA (p.E2476del), BRCA2(NM_000059.4):c.7426_7428delGAA (p.E2476del)
ISCN -
DB-ID BRCA2_001733 See all 8 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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
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.7426_7428del r.(?) p.(Glu2476del) -


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