Variant #0000550700 (NC_000013.10:g.32972744_32972745insGAATTATATC, NM_000059.3:c.10094_10095insGAATTATATC (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.32972744_32972745insGAATTATATC
DNA change (hg38) g.32398607_32398608insGAATTATATC
Published as BRCA2(NM_000059.3):c.10094_10095insGAATTATATC (p.(Ser3366AsnfsTer5)), BRCA2(NM_000059.3):c.10094_10095insGAATTATATC (p.S3366Nfs*5)
ISCN -
DB-ID BRCA2_007087 See all 2 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_NKI
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_NKI
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-05-09 15:51:19 +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.10094_10095insGAATTATATC r.(?) p.(Ser3366AsnfsTer5) -
N4BP2L1 NM_052818.2 ?/. - c.*4334_*4335insGATATAATTC r.(=) p.(=) -


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