Variant #0000000008 (NC_000004.11:g.619654T>C, PDE6B(NM_000283.3):c.239T>C)

Individual ID 00000008
Chromosome 4
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably does not affect function
DNA change (genomic) (Relative to hg19 / GRCh37) g.619654T>C
Reference -
DB-ID PDE6B_000001
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     
PDE6B NM_000283.3 +?/-? - c.239T>C r.? p.Leu80Pro VUS LP



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000008 DNA SEQ-NG PDE6B 1 variome.ir