Variant #0000949931 (NC_000012.11:g.2797598C>A, NC_000012.11(NM_000719.6):c.5785-15C>A (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.2797598C>A
DNA change (hg38) -
Published as CACNA1C(NM_001167623.2):c.5785-15C>A, CACNA1C(NM_199460.4):c.6034-15C>A
ISCN -
DB-ID CACNA1C_000332 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) 3.0E-5 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 2023-11-27 17:35:39 +01:00 (CET)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CACNA1C NM_000719.6 -/. - c.5785-15C>A r.(=) p.(=)
DCP1B NM_152640.3 -/. - c.-684001G>T r.(?) p.(=)
CACNA1C NM_199460.2 -/. - c.6034-15C>A r.(=) p.(=)
CACNA1C-AS1 NR_045725.1 -/. - n.333+1708G>T r.(?) -


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