Variant #0000269809 (NC_000003.11:g.8787317C>T, NM_033337.2:c.220C>T (CAV3))

Chromosome 3
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.8787317C>T
DNA change (hg38) g.8745631C>T
Published as CAV3(NM_033337.2):c.220C>T (p.R74C)
ISCN -
DB-ID CAV3_000083
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 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
OXTR NM_000916.3 ?/. - c.*7346G>A r.(=) p.(=)
SSUH2 NM_015931.2 ?/. - c.-93826G>A r.(?) p.(=)
CAV3 NM_033337.2 ?/. - c.220C>T r.(?) p.(Arg74Cys)


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