Variant #0000619527 (NC_000023.10:g.38182792C>T, NC_000023.10(NM_001034853.1):c.29-15G>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.38182792C>T
DNA change (hg38) g.38323539C>T
Published as -
ISCN -
DB-ID RPGR_000137 See all 6 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) 0.21576 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 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.29-15G>A r.(=) p.(=)
RPGR NM_001034853.1 -/. - c.29-15G>A r.(=) p.(=)


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