Variant #0000255011 (NC_000023.10:g.38182665A>C, NM_001034853.1:c.141T>G (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.38182665A>C
DNA change (hg38) g.38323412A>C
Published as RPGR(NM_001034853.1):c.141T>G (p.S47=), RPGR(NM_001034853.2):c.141T>G (p.S47=)
ISCN -
DB-ID RPGR_000057 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) 0.00051 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-01-20 09:31:28 +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.141T>G r.(?) p.(Ser47=)
RPGR NM_001034853.1 -?/. - c.141T>G r.(?) p.(Ser47=)


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