Variant #0000913824 (NC_000012.11:g.2794977G>A, NM_000719.6:c.5649G>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.2794977G>A
DNA change (hg38) -
Published as CACNA1C(NM_000719.7):c.5649G>A (p.P1883=), CACNA1C(NM_199460.4):c.5898G>A (p.P1966=), CACNA1C-AS1(NR_045725.1):n.333+4329C>T
ISCN -
DB-ID CACNA1C_000137 See all 3 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) 0.02078 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-01-11 15:44:22 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CACNA1C NM_000719.6 -/. - c.5649G>A r.(?) p.(Pro1883=)
DCP1B NM_152640.3 -/. - c.-681380C>T r.(?) p.(=)
CACNA1C NM_199460.2 -/. - c.5898G>A r.(?) p.(Pro1966=)
CACNA1C-AS1 NR_045725.1 -/. - n.333+4329C>T r.(?) -


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