Variant #0000054182 (NC_000017.10:g.41276049A>G, BRCA1(NM_007294.3):c.65T>C)

Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.41276049A>G
DNA change (hg38) g.43124032A>G
Published as L22S
ISCN -
DB-ID BRCA1_000013 See all 6 reported entries
Variant remarks Statistical prediction model; predicted deleterious
Reference PubMed: Sweet 2009
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Peter Devilee
Database submission license No license selected
Created by Maaike Vreeswijk
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
BRCA1 NM_007294.3 +/. 2 c.65T>C r.(?) p.Leu22Ser -