Variant #0000053515 (NC_000013.10:g.32928936A>G, NC_000013.10(NM_000059.3):c.7008-62A>G (BRCA2))

Chromosome 13
Allele Parent #1
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.32928936A>G
DNA change (hg38) g.32354799A>G
Published as -
ISCN -
DB-ID BRCA2_000178 See all 103 reported entries
Variant remarks co-ocurrence; neutral
Reference PubMed: Caputo 2011
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Aura Carreira
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Maaike Vreeswijk
Date created 2012-03-23 17:17:20 +01:00 (CET)
Date last edited 2020-07-03 15:48:03 +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 -?/. 13i c.7008-62A>G r.(=) IVS13-62A>G -


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