Variant #0000923967 (NC_000003.11:g.50403503T>C, NM_006030.2:c.2801A>G (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.50403503T>C
DNA change (hg38) -
Published as CACNA2D2(NM_006030.4):c.2801A>G (p.Q934R)
ISCN -
DB-ID CACNA2D2_000019
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) 0.00039 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-04-16 21:50:28 +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.2801A>G r.(?) p.(Gln934Arg)
NPRL2 NM_006545.4 ?/. - c.-15420A>G r.(?) p.(=)
CYB561D2 NM_007022.3 ?/. - c.*12328T>C r.(=) p.(=)
TMEM115 NM_007024.4 ?/. - c.-7009A>G r.(?) p.(=)


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