Variant #0001010460 (NC_000001.10:g.197390140C>A, NM_201253.2:c.1182C>A (CRB1))

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification pathogenic (recessive)
DNA change (genomic) (Relative to hg19 / GRCh37) g.197390140C>A
DNA change (hg38) g.197421010C>A
Published as -
ISCN -
DB-ID CRB1_000438 See all 3 reported entries
Variant remarks ACMG PVS1, PM2, PP3
Reference -
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner Marta Corton
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2024-09-30 17:29:59 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CRB1 NM_201253.2 +/. 6 c.1182C>A r.(?) p.(Cys394Ter)


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