Variant #0000055776 (NC_000017.10:g.41267810G>A, BRCA1(NM_007294.3):c.81-14C>T)

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.41267810G>A
DNA change (hg38) g.43115793G>A
Published as c.81-14 C>T
ISCN -
DB-ID BRCA1_000021 See all 25 reported entries
Variant remarks splicing reporter minigene/patient RNA analysis; no splicing defect
Reference PubMed: Théry 2011
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00039 View details
Owner Maaike Vreeswijk
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 ?/. 2i c.81-14C>T r.= NA -