Variant #0000862929 (NC_000012.11:g.2017036G>A, NC_000012.11(NM_172364.4):c.649+5C>T (CACNA2D4))

Chromosome 12
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.2017036G>A
DNA change (hg38) -
Published as CACNA2D4(NM_172364.4):c.649+5C>T
ISCN -
DB-ID CACNA2D4_000103
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) 3.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:51:19 +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     
LRTM2 NM_001039029.2 ?/. - c.*73149G>A r.(=) p.(=)
CACNA2D4 NM_172364.4 ?/. - c.649+5C>T r.spl? p.?


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