Variant #0000547334 (NC_000012.11:g.1969369G>A, NM_172364.4:c.1882C>T (CACNA2D4))

Chromosome 12
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.1969369G>A
DNA change (hg38) g.1860203G>A
Published as CACNA2D4(NM_172364.4):c.1882C>T (p.R628*)
ISCN -
DB-ID CACNA2D4_000054 See all 7 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) 0.0008 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 2020-07-02 10:15:06 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LRTM2 NM_001039029.2 +/. - c.*25482G>A r.(=) p.(=)
CACNA2D4 NM_172364.4 +/. - c.1882C>T r.(?) p.(Arg628Ter)


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