Variant #0000790464 (NC_000023.10:g.38163917C>G, NM_001034853.1:c.905G>C (RPGR))

Chromosome X
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.38163917C>G
DNA change (hg38) g.38304664C>G
Published as -
ISCN -
DB-ID RPGR_000134 See all 3 reported entries
Variant remarks -
Reference PubMed: Wang 2014
ClinVar ID -
dbSNP ID rs62640590
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.0009 View details
Owner LOVD
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2021-06-25 14:31:53 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RPGR NM_001034853.1 ?/. - c.905G>C r.(?) p.(Cys302Ser)



Screenings

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