Variant #0000054207 (NC_000017.10:g.41267784G>C, BRCA1(NM_007294.3):c.93C>G)

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.41267784G>C
DNA change (hg38) g.43115767G>C
Published as I31M
ISCN -
DB-ID BRCA1_000025 See all 9 reported entries
Variant remarks protein binding ability BARD1; normal binding
Reference PubMed: Ransburgh 2010
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner Maaike Vreeswijk
Database submission license No license selected
Created by Maaike Vreeswijk
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
BRCA1 NM_007294.3 -?/. 3 c.93C>G r.(?) p.Ile31Met -