Variant #0000055322 (NC_000017.10:g.41215385T>C, NM_007294.3:c.5158A>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.41215385T>C
DNA change (hg38) g.43063368T>C
Published as T1720A
ISCN -
DB-ID BRCA1_000409 See all 33 reported entries
Variant remarks Bayesian statistics; predicted neutral
Reference PubMed: Williams 2003
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00017 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 16:25:01 +02:00 (CEST)
Date last edited 2020-07-13 14:27:31 +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 -/. 19 c.5158A>G r.(?) p.Thr1720Ala -


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