Variant #0000174913 (NC_000003.11:g.8787330C>T, NM_033337.2:c.233C>T (CAV3))

Chromosome 3
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.8787330C>T
DNA change (hg38) g.8745644C>T
Published as -
ISCN -
DB-ID CAV3_000030 See all 26 reported entries
Variant remarks expression cloning COS7-cells, CAV3 expression normal, correctly targeted
Reference PubMed: Traverso 2008
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00262 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2012-04-15 15:58:24 +02:00 (CEST)
Date last edited 2020-07-14 21:50:58 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CAV3 NM_033337.2 ?/. 2 c.233C>T r.(?) p.Thr78Met


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