Variant #0000264329 (NC_000003.11:g.8787499G>C, NM_033337.2:c.402G>C (CAV3))

Chromosome 3
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.8787499G>C
DNA change (hg38) g.8745813G>C
Published as CAV3(NM_033337.3):c.402G>C (p.A134=)
ISCN -
DB-ID CAV3_000090
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) 9.0E-5 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 2018-01-15 20:58:59 +01:00 (CET)
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.*7164C>G r.(=) p.(=)
SSUH2 NM_015931.2 -?/. - c.-94008C>G r.(?) p.(=)
CAV3 NM_033337.2 -?/. - c.402G>C r.(?) p.(Ala134=)


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