Variant #0000054958 (NC_000017.10:g.41223094T>C, NM_007294.3:c.4837A>G (BRCA1))

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.41223094T>C
DNA change (hg38) g.43071077T>C
Published as S1613G
ISCN -
DB-ID BRCA1_000338 See all 1430 reported entries
Variant remarks Transcription activation in human cells; as wildtype control
Reference PubMed: Carvalho 2007
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.3546 View details
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 2020-07-13 14:35:03 +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 -/. 16 c.4837A>G r.(?) p.Ser1613Gly -


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