Variant #0000053285 (NC_000013.10:g.32906729A>C, NM_000059.3:c.1114A>C (BRCA2))

Chromosome 13
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.32906729A>C
DNA change (hg38) g.32332592A>C
Published as 1342A/C (H372N)
ISCN -
DB-ID BRCA2_000052 See all 1062 reported entries
Variant remarks Prevalence in normal controls; predicted neutral
Reference PubMed: Wagner 1999
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.2795 View details
Owner Peter Devilee
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Maaike Vreeswijk
Date created 2009-10-03 17:15:53 +02:00 (CEST)
Date last edited 2020-07-03 15:01:03 +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 -/. 10 c.1114A>C r.(?) p.His372Asn -


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