Variant #0000520768 (NC_000003.11:g.8787514C>T, NM_033337.2:c.417C>T (CAV3))

Chromosome 3
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.8787514C>T
DNA change (hg38) g.8745828C>T
Published as CAV3(NM_033337.3):c.417C>T (p.V139=)
ISCN -
DB-ID CAV3_000100 See all 6 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) 0.00036 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
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     
OXTR NM_000916.3 -/. - c.*7149G>A r.(=) p.(=)
SSUH2 NM_015931.2 -/. - c.-94023G>A r.(?) p.(=)
CAV3 NM_033337.2 -/. - c.417C>T r.(?) p.(Val139=)


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