Variant #0000923968 (NC_000003.11:g.50405113C>T, NM_006030.2:c.2257G>A (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.50405113C>T
DNA change (hg38) -
Published as CACNA2D2(NM_006030.4):c.2257G>A (p.A753T)
ISCN -
DB-ID CACNA2D2_000020
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) 6.0E-5 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.2257G>A r.(?) p.(Ala753Thr)
NPRL2 NM_006545.4 ?/. - c.-17030G>A r.(?) p.(=)
CYB561D2 NM_007022.3 ?/. - c.*13938C>T r.(=) p.(=)
TMEM115 NM_007024.4 ?/. - c.-8619G>A r.(?) p.(=)


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