Variant #0000046106 (NC_000017.10:g.41226488C>A, NM_007294.3:c.4535G>T (BRCA1))

Chromosome 17
Allele Parent #1
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.41226488C>A
DNA change (hg38) g.43074471C>A
Published as 4654G>T
ISCN -
DB-ID BRCA1_000324 See all 56 reported entries
Variant remarks -
Reference UMD BRCA1 database
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00232 View details
Owner UMD
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Julia Lopez
Date created 2014-10-20 13:31:25 +02:00 (CEST)
Date last edited 2017-04-22 20:41:19 +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 -/. 15 c.4535G>T r.(?) p.(Ser1512Ile) -



Screenings

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