Variant #0000980216 (NC_000012.11:g.2797944C>G, NM_000719.6:c.6116C>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.2797944C>G
DNA change (hg38) -
Published as CACNA1C(NM_000719.7):c.6116C>G (p.A2039G), CACNA1C(NM_199460.3):c.6365C>G (p.A2122G), CACNA1C(NM_199460.4):c.6365C>G (p.A2122G)
ISCN -
DB-ID CACNA1C_000143 See all 4 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) 8.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2024-04-19 20:27:30 +02:00 (CEST)
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.6116C>G r.(?) p.(Ala2039Gly)
DCP1B NM_152640.3 ?/. - c.-684347G>C r.(?) p.(=)
CACNA1C NM_199460.2 ?/. - c.6365C>G r.(?) p.(Ala2122Gly)
CACNA1C-AS1 NR_045725.1 ?/. - n.333+1362G>C r.(?) -


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