Variant #0000856585 (NC_000023.10:g.38145658_38145660del, NM_001034853.1:c.2594_2596del (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.38145658_38145660del
DNA change (hg38) -
Published as RPGR(NM_001034853.2):c.2594_2596delGAG (p.G865del)
ISCN -
DB-ID RPGR_000759 See all 4 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) Retrieve
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2022-05-09 15:47:41 +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_000328.2 -?/. - c.1905+689_1905+691del r.(=) p.(=)
RPGR NM_001034853.1 -?/. - c.2594_2596del r.(?) p.(Gly865del)


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