Variant #0000266159 (NC_000013.10:g.32911300_32911303del, NM_000059.3:c.2808_2811del (BRCA2))

Chromosome 13
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.32911300_32911303del
DNA change (hg38) g.32337163_32337166del
Published as BRCA2(NM_000059.3):c.2808_2811del (p.(Ala938ProfsTer21)), BRCA2(NM_000059.3):c.2808_2811delACAA (p.A938Pfs*21), BRCA2(NM_000059.4):c.2808_2811delAC...
ISCN -
DB-ID BRCA2_001211 See all 152 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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
BRCA2 NM_000059.3 +/. - c.2808_2811del r.(?) p.(Ala938ProfsTer21) -


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