Variant #0000619524 (NC_000023.10:g.38163917C>G, NM_001034853.1:c.905G>C (RPGR))

Chromosome X
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.38163917C>G
DNA change (hg38) g.38304664C>G
Published as RPGR(NM_001034853.2):c.905G>C (p.C302S)
ISCN -
DB-ID RPGR_000134 See all 3 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.0009 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2021-01-20 09:31:47 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RPGR NM_000328.2 -/. - c.905G>C r.(?) p.(Cys302Ser)
RPGR NM_001034853.1 -/. - c.905G>C r.(?) p.(Cys302Ser)


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