Variant #0000547755 (NC_000012.11:g.2795412C>T, NM_000719.6:c.5761C>T (CACNA1C))

Chromosome 12
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.2795412C>T
DNA change (hg38) g.2686246C>T
Published as -
ISCN -
DB-ID CACNA1C_000212
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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.5761C>T r.(?) p.(Pro1921Ser)
DCP1B NM_152640.3 -?/. - c.-681815G>A r.(?) p.(=)
CACNA1C NM_199460.2 -?/. - c.6010C>T r.(?) p.(Pro2004Ser)
CACNA1C-AS1 NR_045725.1 -?/. - n.333+3894G>A r.(?) -


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