Variant #0000055547 (NC_000017.10:g.41201130A>G, NC_000017.10(NM_007294.3):c.5406+8T>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.41201130A>G
DNA change (hg38) g.43049113A>G
Published as c.5406+8T>C
ISCN -
DB-ID BRCA1_000457 See all 14 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) 0.00113 View details
Owner Maaike Vreeswijk
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Maaike Vreeswijk
Date created 2014-02-19 14:08:12 +01:00 (CET)
Date last edited 2019-02-25 21:12:28 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
BRCA1 NM_007294.3 ?/. 22i c.5406+8T>C r.= NA -


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