Variant #0000801337 (NC_000003.11:g.53757847G>A, NM_000720.3:c.1981G>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.53757847G>A
DNA change (hg38) -
Published as CACNA1D(NM_001128840.3):c.1921G>A (p.A641T)
ISCN -
DB-ID CACNA1D_000154
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CACNA1D NM_000720.3 ?/. - c.1981G>A r.(?) p.(Ala661Thr)
CACNA1D NM_001128840.2 ?/. - c.1921G>A r.(?) p.(Ala641Thr)


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