Variant #0001010638 (NC_000001.10:g.197396917C>T, NM_201253.2:c.2462C>T (CRB1))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.197396917C>T
DNA change (hg38) g.197427787C>T
Published as -
ISCN -
DB-ID CRB1_000129 See all 7 reported entries
Variant remarks ACMG PM2, PP2, BP6
Reference -
ClinVar ID -
dbSNP ID rs142857810
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00024 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 ?/. 7 c.2462C>T r.(?) p.(Thr821Met)


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