Variant #0000055788 (NC_000017.10:g.41276033C>T, NC_000017.10(NM_007294.3):c.80+1G>A (BRCA1))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.41276033C>T
DNA change (hg38) g.43124016C>T
Published as 199+1G>A
ISCN -
DB-ID BRCA1_000553 See all 8 reported entries
Variant remarks Splicing reporter minigene; predicted deleterious, Use of cryptic splice site in intron 5
Reference PubMed: Steffensen 2014
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Maaike Vreeswijk
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Maaike Vreeswijk
Date created 2014-02-19 14:51:59 +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 +?/. 2i c.80+1G>A r.del ? -


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