Variant #0000829632 (NC_000006.11:g.42672273G>A, NM_000322.4:c.658C>T (PRPH2))

Chromosome 6
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.42672273G>A
DNA change (hg38) -
Published as c.658C>T/p.R220W
ISCN -
DB-ID PRPH2_000023 See all 20 reported entries
Variant remarks leads to pattern dystrophy
Reference PubMed: Becirovic-2016
ClinVar ID -
dbSNP ID -
Origin In silico
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner LOVD
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Julia Lopez
Date created 2021-12-15 12:47:34 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRPH2 NM_000322.4 +/. 2 c.658C>T r.(?) p.Arg220Trp


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