Variant #0000719252 (NC_000003.11:g.150690347_150690348insGACA, NM_174878.2:c.148_149insTGTC (CLRN1))

Chromosome 3
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.150690347_150690348insGACA
DNA change (hg38) -
Published as CLRN1(NM_001256819.1):c.148_149insTGTC (p.S50Lfs*12)
ISCN -
DB-ID CLRN1_000253
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) 0.0001 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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
CLRN1 NM_001195794.1 +/. - c.148_149insTGTC r.(?) p.(Ser50Leufs*12) -
CLRN1 NM_174878.2 +/. - c.148_149insTGTC r.(?) p.(Ser50Leufs*12) -


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