Variant #0000055351 (NC_000017.10:g.41209139A>G, NM_007294.3:c.5207T>C (BRCA1))

Chromosome 17
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.41209139A>G
DNA change (hg38) g.43057122A>G
Published as V1736A
ISCN -
DB-ID BRCA1_000420 See all 24 reported entries
Variant remarks Thermodynamic stability prediction; moderately destabilizing
Reference PubMed: Rowling 2010
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Hilmi Ozcelik
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Maaike Vreeswijk
Date created 2011-09-29 17:53:56 +02:00 (CEST)
Date last edited 2020-07-13 14:26:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
BRCA1 NM_007294.3 ?/. 20 c.5207T>C r.(?) p.Val1736Ala -


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