Variant #0000007226 (NC_000017.11:g.61686104T>C, BRIP1(NM_032043.2):c.2637A>G)

Individual ID 00001281
Chromosome 17
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Probably does not affect function
DNA change (genomic) (Relative to hg38 / GRCh38) g.61686104T>C
Reference -
DB-ID BRIP1_000001 See all 28 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     

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Review status     
BRIP1 NM_032043.2 ./-? 19 c.2637A>G p.(=) Not specified no r.(=) -



Screenings


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Owner     
0000001520 DNA CNV;SEQ-NG IACA Panel (ATM, BARD1, BRCA1, BRCA2, BRIP1, CDH1, CHEK2, EPCAM, MLH1, MSH2, MSH6, MUTYH, NBN, PALB2, PMS2, PPM1D, PTEN, RAD51C, RAD51D, STK11, TP53) 10-jan-2020 Multigenetic panel - 36 Silvina Sisterna-Hospital de Comunidad