Variant #0000000047 (NC_000016.9:g.56536655delG, BBS2(NM_031885.3):c.870delC)

Individual ID 00000065
Chromosome 16
Allele Both (homozygous)
Affects function (as reported) Affects function
Affects function (by curator) Affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.56536655delG
Reference -
DB-ID BBS2_000002
Average frequency (gnomAD v.2.1.1) Retrieve
Owner variome.ir
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by variome.ir
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Classification     
BBS2 NM_031885.3 +/+ - c.870delC r.(?) p.(Gly291Valfs*3) Pathogenic



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000065 DNA SEQ-NG BBS2 1 variome.ir