Variant #0000532758 (NC_000007.13:g.81679904T>A, NC_000007.13(NM_000722.2):c.879+9840A>T (CACNA2D1))

Chromosome 7
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.81679904T>A
DNA change (hg38) g.82050588T>A
Published as CACNA2D1(NM_001302890.2):c.920A>T (p.N307I)
ISCN -
DB-ID CACNA2D1_000098 See all 2 reported entries
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2019-12-04 15:24:38 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CACNA2D1 NM_000722.2 -/. - c.879+9840A>T r.(=) p.(=)


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