Variant #0000993792 (NC_000003.11:g.50388062C>A, NM_006030.2:c.*14035G>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.50388062C>A
DNA change (hg38) -
Published as NPRL2(NM_006545.4):c.22G>T (p.(Glu8*))
ISCN -
DB-ID CACNA2D2_000025
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +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     
CACNA2D2 NM_006030.2 ?/. - c.*14035G>T r.(=) p.(=)
NPRL2 NM_006545.4 ?/. - c.22G>T r.(?) p.(Glu8*)
CYB561D2 NM_007022.3 ?/. - c.-445C>A r.(?) p.(=)
TMEM115 NM_007024.4 ?/. - c.*4712G>T r.(=) p.(=)
ZMYND10 NM_015896.2 ?/. - c.-5052G>T r.(?) p.(=)


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