Variant #0000000048 (NC_000006.11:g.42672135C>A, PRPH2(NM_000322.4):c.796G>T)

Individual ID 00000067
Chromosome 6
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.42672135C>A
Reference -
DB-ID PRPH2_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     
PRPH2 NM_000322.4 +/+ - c.796G>T r.(?) p.(Gly266Cys) Likely Pathogenic



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000067 DNA SEQ-NG PRPH2 1 variome.ir