Variant #0000000022 (NC_000014.8:g.21762926_21762927insGGTGAAG, RPGRIP1(NM_020366.3):c.176_177insGGTGAAG)

Individual ID 00000024
Chromosome 14
Allele Both (homozygous)
Affects function (as reported) Affects function
Affects function (by curator) Affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.21762926_21762927insGGTGAAG
Reference -
DB-ID RPGRIP1_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     
RPGRIP1 NM_020366.3 +/+ - c.176_177insGGTGAAG r.(?) p.(Glu62Glyfs*11) Pathogenic



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000025 DNA SEQ-NG RPGRIP1 1 variome.ir