Variant #0000191600 (NC_000013.10:g.32907514_32907515insTT, NM_000059.3:c.1899_1900insTT (BRCA2))

Chromosome 13
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification pathogenic (dominant)
DNA change (genomic) (Relative to hg19 / GRCh37) g.32907514_32907515insTT
DNA change (hg38) g.32333377_32333378insTT
Published as 1899_1900insTT
ISCN -
DB-ID BRCA2_001248 See all 23 reported entries
Variant remarks Variant allele predicted to encode truncated non-functional protein
Reference ENIGMA classification criteria
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner ENIGMA consortium
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by ENIGMA consortium
Date created 2016-09-08 12:00:00 +02:00 (CEST)
Date last edited 2020-02-20 16:18:07 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
BRCA2 NM_000059.3 +/+ 10 c.1899_1900insTT r.(?) p.(Ala634Leufs*11) -


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.