Variant #0000000034 (NC_000014.8:g.68196003_68196004insC, RDH12(NM_152443.2):c.754_755insC)

Individual ID 00000047
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.68196003_68196004insC
Reference -
DB-ID RDH12_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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Classification     
RDH12 NM_152443.2 +/+ - c.754_755insC r.(?) p.(Phe254Leufs*19) Pathogenic



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000047 DNA SEQ-NG RDH12 1 variome.ir