Variant #0000520417 (NC_000003.11:g.53699675dup, NC_000003.11(NM_000720.3):c.767-12dup (CACNA1D))

Chromosome 3
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.53699675dup
DNA change (hg38) g.53665648dup
Published as CACNA1D(NM_000720.4):c.767-12dupT
ISCN -
DB-ID CACNA1D_000101 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 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CACNA1D NM_000720.3 -/. - c.767-12dup r.(=) p.(=)
CACNA1D NM_001128840.2 -/. - c.767-12dup r.(=) p.(=)


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