Variant #0000896200 (NC_000023.10:g.38186672G>T, NM_001034853.1:c.-52C>A (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.38186672G>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID RPGR_000811
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) 0.01501 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2022-11-01 13:41:49 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RPGR NM_000328.2 -/. - c.-52C>A r.(?) p.(=)
RPGR NM_001034853.1 -/. - c.-52C>A r.(?) p.(=)


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