Variant #0000264039 (NC_000003.11:g.53531380_53531383del, NM_000720.3:c.269_272del (CACNA1D))

Chromosome 3
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.53531380_53531383del
DNA change (hg38) g.53497353_53497356del
Published as CACNA1D(NM_000720.4):c.269_272delAGAG (p.K90Tfs*32)
ISCN -
DB-ID CACNA1D_000020
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CACNA1D NM_000720.3 -?/. - c.269_272del r.(?) p.(Lys90ThrfsTer32)
CACNA1D NM_001128840.2 -?/. - c.269_272del r.(?) p.(Lys90ThrfsTer32)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.