Variant #0000677070 (NC_000003.11:g.53707848G>A, NC_000003.11(NM_000720.3):c.1220+5G>A (CACNA1D))

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.53707848G>A
DNA change (hg38) -
Published as CACNA1D(NM_001128840.3):c.1220+695G>A
ISCN -
DB-ID CACNA1D_000149
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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CACNA1D NM_000720.3 ?/. - c.1220+5G>A r.spl? p.?
CACNA1D NM_001128840.2 ?/. - c.1220+695G>A r.(=) p.(=)


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