Variant #0000949932 (NC_000012.11:g.2797846C>A, NM_000719.6:c.6018C>A (CACNA1C))

Chromosome 12
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.2797846C>A
DNA change (hg38) -
Published as CACNA1C(NM_000719.6):c.6018C>A (p.(Ser2006Arg)), CACNA1C(NM_199460.4):c.6267C>A (p.S2089R)
ISCN -
DB-ID CACNA1C_000333 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 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 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CACNA1C NM_000719.6 ?/. - c.6018C>A r.(?) p.(Ser2006Arg)
DCP1B NM_152640.3 ?/. - c.-684249G>T r.(?) p.(=)
CACNA1C NM_199460.2 ?/. - c.6267C>A r.(?) p.(Ser2089Arg)
CACNA1C-AS1 NR_045725.1 ?/. - n.333+1460G>T r.(?) -


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