Variant #0000928829 (NC_000003.11:g.8787196C>T, NC_000003.11(NM_033337.2):c.115-16C>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.8787196C>T
DNA change (hg38) -
Published as CAV3(NM_033337.3):c.115-16C>T
ISCN -
DB-ID CAV3_000137
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) Retrieve
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2023-07-07 10:10:56 +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     
OXTR NM_000916.3 -/. - c.*7467G>A r.(=) p.(=)
SSUH2 NM_015931.2 -/. - c.-93705G>A r.(?) p.(=)
CAV3 NM_033337.2 -/. - c.115-16C>T r.(=) p.(=)


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