Variant #0000859092 (NC_000003.11:g.50385819G>A, NM_006030.2:c.*16278C>T (CACNA2D2))

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.50385819G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID CACNA2D2_000014
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CACNA2D2 NM_006030.2 ?/. - c.*16278C>T r.(=) p.(=)
NPRL2 NM_006545.4 ?/. - c.743C>T r.(?) p.(Thr248Met)
CYB561D2 NM_007022.3 ?/. - c.-2688G>A r.(?) p.(=)
TMEM115 NM_007024.4 ?/. - c.*6955C>T r.(=) p.(=)
ZMYND10 NM_015896.2 ?/. - c.-2809C>T r.(?) p.(=)


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