Variant #0000053241 (NC_000013.10:g.32900405C>A, NM_000059.3:c.502C>A (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.32900405C>A
DNA change (hg38) g.32326268C>A
Published as P168T
ISCN -
DB-ID BRCA2_000033 See all 13 reported entries
Variant remarks Multifactorial likelihood-ratio model; predicted neutral
Reference PubMed: Easton 2007
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 4.0E-5 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 14:54:15 +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 -/. 6 c.502C>A r.(?) p.Pro168Thr -


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