Variant #0000054913 (NC_000017.10:g.41226601G>C, NC_000017.10(NM_007294.3):c.4485-63C>G (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.41226601G>C
DNA change (hg38) g.43074584G>C
Published as IVS14-63A/G
ISCN -
DB-ID BRCA1_000321 See all 70 reported entries
Variant remarks -
Reference PubMed: Diez 2003
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Peter Devilee
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Maaike Vreeswijk
Date created 2009-10-03 16:25:00 +02:00 (CEST)
Date last edited 2019-02-07 08:31:26 +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 ?/. 14i c.4485-63C>G r.(?) ? -


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