Variant #0000520423 (NC_000003.11:g.53757865A>T, NM_000720.3:c.1999A>T (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.53757865A>T
DNA change (hg38) g.53723838A>T
Published as CACNA1D(NM_000720.3):c.1999A>T (p.M667L), CACNA1D(NM_000720.4):c.1999A>T (p.M667L)
ISCN -
DB-ID CACNA1D_000041 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) 5.0E-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 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.1999A>T r.(?) p.(Met667Leu)
CACNA1D NM_001128840.2 ?/. - c.1939A>T r.(?) p.(Met647Leu)


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