Variant #0000054193 (NC_000017.10:g.41267809G>C, BRCA1(NM_007294.3):c.81-13C>G)

Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.41267809G>C
DNA change (hg38) g.43115792G>C
Published as IVS2-13C>G
ISCN -
DB-ID BRCA1_000020 See all 13 reported entries
Variant remarks Multifactorial likelihood-ratio model; predicted neutral
Reference PubMed: Easton 2007
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00018 View details
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 -/. 2i c.81-13C>G r.(=) ? -