Variant #0000055787 (NC_000017.10:g.41276163_41276164dup, NC_000017.10(NM_007294.3):c.-19-22_-19-21dup (BRCA1))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.41276163_41276164dup
DNA change (hg38) g.43124146_43124147dup
Published as 101-21insAT
ISCN -
DB-ID BRCA1_000552 See all 6 reported entries
Variant remarks Splicing reporter minigene; predicted neutral, Use of cryptic splice site in exon 3
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 2020-07-13 15:54:57 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
BRCA1 NM_007294.3 -?/. 1i c.-19-22_-19-21dup r.= ? -


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