Variant #0000016598 (NC_000016.9:g.53726113T>A, NM_015272.2:c.394A>T (RPGRIP1L))

Chromosome 16
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic (recessive)
DNA change (genomic) (Relative to hg19 / GRCh37) g.53726113T>A
DNA change (hg38) g.53692201T>A
Published as R132X
ISCN -
DB-ID RPGRIP1L_000013 See all 3 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs121918201
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Anne Polvi
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Anne Polvi
Date created 2012-12-04 16:00:56 +01:00 (CET)
Date last edited 2023-11-28 16:07:42 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RPGRIP1L NM_015272.2 +/. 4 c.394A>T r.(394a>u) p.(Arg132*)


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