Overview

Variant ID 29550
Entrez Gene ID 775
Gene CACNA1C (GeneCards)
Location hg19 12:2717804-2717804
hg38 12:2608638-2608638
Disease Autism Spectrum Disorders (view all the variants in this disease)
Method MiSeq
Mutation(HGVS format) NC_000012.11:g.2717804 G>C (Genome Assembly: hg19)

Other information

Exon or Intron NA
Position in protein NA
Amino acid changes in protein NA > NA
Position in cDNA NA
Changes in cDNA NA > NA
mRNA accession NA
mRNA length NA
Reference length 133851895

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score 0.834
CADD Raw score (version 1.3) 6.411651 (Deleterious)
FATHMM raw prediction score 0.98829 (Tolerated)
SIFT score 0.025 (Deleterious)
LRT score 0 (Deleterious)
MutationTaster score 1 (Deleterious)
MutatioinAssessor score 2.145 (Deleterious)
PROVEAN score -2.79 (Deleterious)
MetaSVM score 1.107 (Deleterious)
MetaLR score 0.955 (Deleterious)
MCAP score 0.859 (Deleterious)
FitCons score 0.516 (Highly Significant p < 0.003 )
Genomic Evolutionary Rate Profiling (GERP) score 4.74
PhyloP score based on multiple alignment of 100 vertebrates 9.602
PhastCons score based on multiple alignment of 100 vertebrates 1
SiPhy log transformed odds ratio on multiple alignment of 29 mammals 18.275
Deleterious probability by iFish2 0.7328 (Deleterious)
Deleterious probability by DeFine 0.9657 (Deleterious)
Entrez Gene ID 775 (NCBI Gene)
Official Gene Symbol CACNA1C (GeneCards)
Number of variants in CACNA1C in this database 8 (view all the variants)
Full name calcium voltage-gated channel subunit alpha1 C
Band 12p13.33
Other IDs Vega: OTTHUMG00000150243
OMIM: 114205
HGNC: HGNC:1390
Ensembl: ENSG00000151067
Other names TS, LQT8, CACH2, CACN2, CaV1.2, CCHL1A1, CACNL1A1
Summary This gene encodes an alpha-1 subunit of a voltage-dependent calcium channel. Calcium channels mediate the influx of calcium ions into the cell upon membrane polarization. The alpha-1 subunit consists of 24 transmembrane segments and forms the pore through which ions pass into the cell. The calcium channel consists of a complex of alpha-1, alpha-2/delta, beta, and gamma subunits in a 1:1:1:1 ratio. There are multiple isoforms of each of these proteins, either encoded by different genes or the result of alternative splicing of transcripts. The protein encoded by this gene binds to and is inhibited by dihydropyridine. Alternative splicing results in many transcript variants encoding different proteins. Some of the predicted proteins may not produce functional ion channel subunits. [provided by RefSeq, Oct 2012]

Individual #1

Individual ID 28714951.226 (view all the variants in this individual)
Pubmed ID 28714951
Whose mosaic mutation Patient  
Phenotype 3  
Disease Autism Spectrum Disorders (view all the variants in this disease)
OMIM ID 209850

Publication #1: 28714951

Pubmed ID 28714951
Title Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder
Journal Nat Neurosci
Publication date 2017.07
Disease Autism Spectrum Disorders
Incidence 0.01
Number of cases cases of unknown sex: 376;