Variant #0000002357 (NC_000017.10:-, BRIP1(NM_032043.2):c.?)

Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type Tissue
DNA change (genomic) (Relative to hg19 / GRCh37) -
Reference GenBank
DB-ID BRIP1_00005
Frequency -
Variant remarks IVS17+2insT ex17del/R831fsX3d
ClassClinical -
Average frequency (gnomAD v.2.1.1) Genomic location of variant could not be determined
Owner Qi Ming
Database submission license No license selected
Created by Qi Ming




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BRIP1 NM_032043.2 ./. 17 c.? - -