Variant #0000534981 (NC_000008.10:g.55538727_55538731del, NM_006269.1:c.2285_2289del (RP1))

Chromosome 8
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.55538727_55538731del
DNA change (hg38) g.54626167_54626171del
Published as RP1(NM_006269.1):c.2285_2289delTAAAT (p.L762Yfs*17), RP1(NM_006269.2):c.2285_2289delTAAAT (p.L762Yfs*17)
ISCN -
DB-ID RP1_000053 See all 40 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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RP1 NM_006269.1 +/. - c.2285_2289del r.(?) p.(Leu762TyrfsTer17)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.