Variant #0000054995 (NC_000017.10:g.41222975C>T, NM_007294.3:c.4956G>A (BRCA1))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.41222975C>T
DNA change (hg38) g.43070958C>T
Published as M1652I
ISCN -
DB-ID BRCA1_000348 See all 152 reported entries
Variant remarks LOH analysis; loss of variant allele
Reference PubMed: Beristain 2010
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.01825 View details
Owner Maaike Vreeswijk
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Maaike Vreeswijk
Date created 2011-08-09 09:15:06 +02:00 (CEST)
Date last edited 2020-07-13 14:34:03 +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.4956G>A r.(?) p.Met1652Ile -


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