Variant #0000890520 (NC_000012.11:g.2795370C>T, NM_000719.6:c.5719C>T (CACNA1C))

Chromosome 12
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.2795370C>T
DNA change (hg38) -
Published as CACNA1C(NM_001167623.2):c.5719C>T (p.Q1907*)
ISCN -
DB-ID CACNA1C_000318
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2022-11-01 13:01:21 +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.5719C>T r.(?) p.(Gln1907*)
DCP1B NM_152640.3 +?/. - c.-681773G>A r.(?) p.(=)
CACNA1C NM_199460.2 +?/. - c.5968C>T r.(?) p.(Gln1990*)
CACNA1C-AS1 NR_045725.1 +?/. - n.333+3936G>A r.(?) -


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