Variant #0000000042 (NC_000023.10:g.46696544_46696546del, RP2(NM_006915.2):c.9_11del)

Individual ID 00000016
Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.46696544_46696546del
Reference -
DB-ID RP2_000001
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Saeed Reza Ghaffari
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Saeed Reza Ghaffari
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Classification     
RP2 NM_006915.2 +/+ - c.9_11del r.(?) p.(Phe5del) Pathogenic



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000017 DNA SEQ-NG RP2 1 variome.ir