Variant #0000007701 (NC_000017.11:g.43082453A>G, BRCA1(NM_007294.3):c.4308T>C)

Individual ID 00001303
Chromosome 17
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Does not affect function
DNA change (genomic) (Relative to hg38 / GRCh38) g.43082453A>G
Reference -
DB-ID BRCA1_000008 See all 287 reported entries
dbSNP ID -
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Silvina Sisterna-Hospital de Comunidad
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Instituto Nacional del Cancer
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

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Co_ocurrence     

Review status     
BRCA1 NM_007294.3 ./- 13 c.4308T>C r.(=) p.(=) Not specified no -



Screenings


AscendingScreening ID     

Template     

Technique     

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Remarks     

Date of test     

Type of test     

Genes screened     

Variants found     

Owner     
0000001542 DNA CNV;SEQ-NG IACA - 21-oct-2019 Multigenetic panel ATM, BRCA1, BRCA2, BRIP1, CDH1, CHEK2, FANCC, NBN, PALB2, PTEN, RAD51C, RAD51D, STK11, TP53 21 Silvina Sisterna-Hospital de Comunidad