Variant #0000269564 (NC_000012.11:g.2224449G>A, NM_000719.6:c.109G>A (CACNA1C))

Chromosome 12
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.2224449G>A
DNA change (hg38) g.2115283G>A
Published as CACNA1C(NM_000719.7):c.109G>A (p.(Gly37Arg), p.G37R), CACNA1C(NM_199460.3):c.109G>A (p.G37R), CACNA1C(NM_199460.4):c.109G>A (p.G37R)
ISCN -
DB-ID CACNA1C_000020 See all 5 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) 0.00352 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +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.109G>A r.(?) p.(Gly37Arg)
DCP1B NM_152640.3 -/. - c.-110852C>T r.(?) p.(=)
CACNA1C NM_199460.2 -/. - c.109G>A r.(?) p.(Gly37Arg)


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