Variant #0000682416 (NC_000023.10:g.38186612C>T, NM_001034853.1:c.9G>A (RPGR))

Chromosome X
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.38186612C>T
DNA change (hg38) -
Published as RPGR(NM_001034853.1):c.9G>A (p.E3=)
ISCN -
DB-ID RPGR_000158
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) 8.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-08-06 14:59:34 +02:00 (CEST)
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.9G>A r.(?) p.(Glu3=)
RPGR NM_001034853.1 -?/. - c.9G>A r.(?) p.(Glu3=)


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