Variant #0000263920 (NC_000012.11:g.2614070G>T, NM_000719.6:c.1176G>T (CACNA1C))

Chromosome 12
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.2614070G>T
DNA change (hg38) g.2504904G>T
Published as CACNA1C(NM_199460.4):c.1176G>T (p.G392=)
ISCN -
DB-ID CACNA1C_000046 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) 0.00196 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 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     
CACNA1C NM_000719.6 -/. - c.1176G>T r.(?) p.(Gly392=)
DCP1B NM_152640.3 -/. - c.-500473C>A r.(?) p.(=)
CACNA1C NM_199460.2 -/. - c.1176G>T r.(?) p.(Gly392=)


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