Variant #0000000067 (NC_000008.10:g.55537940_55537941delAT, RP1(NM_006269.1):c.1498_1499delAT)

Individual ID 00000089
Chromosome 8
Allele Both (homozygous)
Affects function (as reported) Affects function
Affects function (by curator) Affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.55537940_55537941delAT
Reference -
DB-ID RP1_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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Classification     
RP1 NM_006269.1 +/+ - c.1498_1499delAT r.(?) p.(Met500Valfs*7) Pathogenic



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000090 DNA SEQ-NG RP1 1 variome.ir