Variant #0000547671 (NC_000012.11:g.2614110G>A, NM_000719.6:c.1216G>A (CACNA1C))

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.2614110G>A
DNA change (hg38) g.2504944G>A
Published as CACNA1C(NM_000719.6):c.1216G>A (p.(Gly406Arg))
ISCN -
DB-ID CACNA1C_000160 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) Retrieve
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-05-09 15:51:19 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CACNA1C NM_000719.6 +/. - c.1216G>A r.(?) p.(Gly406Arg)
DCP1B NM_152640.3 +/. - c.-500513C>T r.(?) p.(=)
CACNA1C NM_199460.2 +/. - c.1216G>A r.(?) p.(Gly406Arg)


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