Variant #0000622862 (NC_000012.11:g.2791781A>G, NM_000719.6:c.5510A>G (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.2791781A>G
DNA change (hg38) g.2682615A>G
Published as CACNA1C(NM_001167623.2):c.5510A>G (p.Y1837C)
ISCN -
DB-ID CACNA1C_000248
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +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.5510A>G r.(?) p.(Tyr1837Cys)
DCP1B NM_152640.3 ?/. - c.-678184T>C r.(?) p.(=)
CACNA1C NM_199460.2 ?/. - c.5759A>G r.(?) p.(Tyr1920Cys)
CACNA1C-AS1 NR_045725.1 ?/. - n.334-4718T>C r.(?) -


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