Variant #0000055641 (NC_000017.10:g.41199693G>C, NM_007294.3:c.5434C>G (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.41199693G>C
DNA change (hg38) g.43047676G>C
Published as P1812A
ISCN -
DB-ID BRCA1_000478 See all 12 reported entries
Variant remarks Thermostability assay; inconclusive
Reference PubMed: Drikos 2009
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 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 16:25:01 +02:00 (CEST)
Date last edited 2020-07-13 14:16:28 +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 ?/. 23 c.5434C>G r.(?) p.Prol1812Ala -


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