Variant #0000520766 (NC_000003.11:g.8787374G>A, NM_033337.2:c.277G>A (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.8787374G>A
DNA change (hg38) g.8745688G>A
Published as CAV3(NM_033337.2):c.277G>A (p.A93T), CAV3(NM_033337.3):c.277G>A (p.A93T)
ISCN -
DB-ID CAV3_000012 See all 16 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) 0.00015 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +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.*7289C>T r.(=) p.(=)
SSUH2 NM_015931.2 ?/. - c.-93883C>T r.(?) p.(=)
CAV3 NM_033337.2 ?/. - c.277G>A r.(?) p.(Ala93Thr)


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