Variant #0000016603 (NC_000016.9:g.53720397_53720400del, NM_015272.2:c.723_726del (RPGRIP1L))

Chromosome 16
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.53720397_53720400del
DNA change (hg38) g.53686485_53686488del
Published as c.721-4delAATG: p.N241fsX25
ISCN -
DB-ID RPGRIP1L_000008
Variant remarks 1 English MKS5 family (com-het)
Reference PubMed: Otto 2011
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation yes
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 2020-07-09 16:29:39 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RPGRIP1L NM_015272.2 +/+ 6 c.723_726del r.(723_726del) p.(Asn241Lysfs*25)


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