Variant #0000054504 (NC_000017.10:g.41246092A>G, NM_007294.3:c.1456T>C (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.41246092A>G
DNA change (hg38) g.43094075A>G
Published as F486L
ISCN -
DB-ID BRCA1_000150 See all 43 reported entries
Variant remarks co-occurrence with deleterious variant; predicted neutral
Reference PubMed: Judkins 2005b
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00028 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 16:24:59 +02:00 (CEST)
Date last edited 2020-07-13 15:30:13 +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 -/. 11 c.1456T>C r.(?) p.Phe486Leu -


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