Variant #0000859147 (NC_000003.11:g.8787266G>A, NM_033337.2:c.169G>A (CAV3))

Chromosome 3
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.8787266G>A
DNA change (hg38) -
Published as CAV3(NM_001234.3):c.169G>A (p.(Val57Met))
ISCN -
DB-ID CAV3_000015 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) 1.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
OXTR NM_000916.3 +?/. - c.*7397C>T r.(=) p.(=)
SSUH2 NM_015931.2 +?/. - c.-93775C>T r.(?) p.(=)
CAV3 NM_033337.2 +?/. - c.169G>A r.(?) p.(Val57Met)


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