Variant #0000005236 (NC_000017.11:g.43092418T>C, BRCA1(NM_007294.3):c.3113A>G)

Individual ID 00000678
Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Does not affect function
DNA change (genomic) (Relative to hg38 / GRCh38) g.43092418T>C
Reference -
DB-ID BRCA1_000006 See all 296 reported entries
dbSNP ID -
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Lina Nuñez-Hospital Alemán
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Instituto Nacional del Cancer
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Zygosity     

Co_ocurrence     

Review status     
BRCA1 NM_007294.3 -/- 11 c.3113A>G r.(?) p.(Glu1038Gly) Hetero no -



Screenings


AscendingScreening ID     

Template     

Technique     

Lab     

Remarks     

Date of test     

Type of test     

Genes screened     

Variants found     

Owner     
0000000787 DNA SEQ-NG Hidalgo - 27-sep-2018 Specific pathology panel BRCA1, BRCA2 11 Lina Nuñez-Hospital Alemán