Variant #0000520456 (NC_000003.11:g.53845391G>A, NM_000720.3:c.6504G>A (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.53845391G>A
DNA change (hg38) g.53811364G>A
Published as CACNA1D(NM_000720.4):c.6504G>A (p.E2168=), CACNA1D(NM_001128840.3):c.6444G>A (p.E2148=)
ISCN -
DB-ID CHDH_000003 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) 0.00028 View details
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.6504G>A r.(?) p.(Glu2168=)
CACNA1D NM_001128840.2 -/. - c.6444G>A r.(?) p.(Glu2148=)
CHDH NM_018397.4 -/. - c.*6413C>T r.(=) p.(=)


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