12-2053563-A-G

Variant names:

• chr12-2053563-A-G
• NM_000719.7:c.1A>G

Variant summary

Our verdict is Uncertain significance. Variant got 3 ACMG points: 3P and 0B. PVS1_Supporting PM2

The NM_000719.7(CACNA1C):​c.1A>G​(p.Met1?) variant causes a start lost change. The variant allele was found at a frequency of 0.00000138 in 1,444,082 control chromosomes in the GnomAD database, with no homozygous occurrence. In-silico tool predicts a pathogenic outcome for this variant. Variant has been reported in ClinVar as Uncertain significance (★).

• Frequency:
  • Genomes: not found (cov: 31)
  • Exomes 𝑓: 0.0000014 (0 hom.)
• Consequence: CACNA1C NM_000719.7 start_lost
• Clinical Significance: Uncertain significance criteria provided, single submitter U:1
• Conservation: PhyloP100: 3.83

Genes affected

CACNA1C (HGNC:1390): (calcium voltage-gated channel subunit alpha1 C) 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]

ACMG classification

Verdict is Uncertain_significance. Variant got 3 ACMG points.

• PVS1: Start lost variant, no pathogenic variants between lost start and next in-frame start position. Next in-frame start position is after 8 codons. Genomic position: 2053584. Lost 0.003 part of the original CDS.
• PM2: Very rare variant in population databases, with high coverage

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
CACNA1C	NM_000719.7	c.1A>G	p.Met1?	start_lost	Exon 1 of 47	ENST00000399655.6	NP_000710.5
CACNA1C	NM_001167623.2	c.1A>G	p.Met1?	start_lost	Exon 1 of 47	ENST00000399603.6	NP_001161095.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
CACNA1C	ENST00000399603.6	c.1A>G	p.Met1?	start_lost	Exon 1 of 47	5	NM_001167623.2	ENSP00000382512.1
CACNA1C	ENST00000399655.6	c.1A>G	p.Met1?	start_lost	Exon 1 of 47	1	NM_000719.7	ENSP00000382563.1
CACNA1C	ENST00000406454.8	c.1A>G	p.Met1?	start_lost	Exon 1 of 48	5		ENSP00000385896.3
CACNA1C	ENST00000399634.6	c.1A>G	p.Met1?	start_lost	Exon 1 of 47	5		ENSP00000382542.2
CACNA1C	ENST00000347598.9	c.1A>G	p.Met1?	start_lost	Exon 1 of 49	1		ENSP00000266376.6
CACNA1C	ENST00000344100.7	c.1A>G	p.Met1?	start_lost	Exon 1 of 47	1		ENSP00000341092.3
CACNA1C	ENST00000327702.12	c.1A>G	p.Met1?	start_lost	Exon 1 of 48	1		ENSP00000329877.7
CACNA1C	ENST00000399617.6	c.1A>G	p.Met1?	start_lost	Exon 1 of 48	5		ENSP00000382526.1
CACNA1C	ENST00000399638.5	c.1A>G	p.Met1?	start_lost	Exon 1 of 48	1		ENSP00000382547.1
CACNA1C	ENST00000335762.10	c.1A>G	p.Met1?	start_lost	Exon 1 of 48	5		ENSP00000336982.5
CACNA1C	ENST00000399606.5	c.1A>G	p.Met1?	start_lost	Exon 1 of 48	1		ENSP00000382515.1
CACNA1C	ENST00000399621.5	c.1A>G	p.Met1?	start_lost	Exon 1 of 47	1		ENSP00000382530.1
CACNA1C	ENST00000399637.5	c.1A>G	p.Met1?	start_lost	Exon 1 of 47	1		ENSP00000382546.1
CACNA1C	ENST00000402845.7	c.1A>G	p.Met1?	start_lost	Exon 1 of 47	1		ENSP00000385724.3
CACNA1C	ENST00000399629.5	c.1A>G	p.Met1?	start_lost	Exon 1 of 47	1		ENSP00000382537.1
CACNA1C	ENST00000682336.1	c.1A>G	p.Met1?	start_lost	Exon 1 of 47			ENSP00000507898.1
CACNA1C	ENST00000399591.5	c.1A>G	p.Met1?	start_lost	Exon 1 of 46	1		ENSP00000382500.1
CACNA1C	ENST00000399595.5	c.1A>G	p.Met1?	start_lost	Exon 1 of 46	1		ENSP00000382504.1
CACNA1C	ENST00000399649.5	c.1A>G	p.Met1?	start_lost	Exon 1 of 46	1		ENSP00000382557.1
CACNA1C	ENST00000399597.5	c.1A>G	p.Met1?	start_lost	Exon 1 of 47	1		ENSP00000382506.1
CACNA1C	ENST00000399601.5	c.1A>G	p.Met1?	start_lost	Exon 1 of 47	1		ENSP00000382510.1
CACNA1C	ENST00000399641.6	c.1A>G	p.Met1?	start_lost	Exon 1 of 47	1		ENSP00000382549.1
CACNA1C	ENST00000399644.5	c.1A>G	p.Met1?	start_lost	Exon 1 of 47	1		ENSP00000382552.1
CACNA1C	ENST00000682835.1	c.1A>G	p.Met1?	start_lost	Exon 1 of 47			ENSP00000507282.1
CACNA1C	ENST00000683482.1	c.1A>G	p.Met1?	start_lost	Exon 1 of 47			ENSP00000507169.1
CACNA1C	ENST00000682686.1	c.1A>G	p.Met1?	start_lost	Exon 1 of 46			ENSP00000507309.1
CACNA1C	ENST00000682544.1	c.140-61661A>G		intron_variant	Intron 1 of 49			ENSP00000507184.1
CACNA1C	ENST00000683824.1	c.140-61661A>G		intron_variant	Intron 1 of 47			ENSP00000507867.1
CACNA1C	ENST00000682462.1	c.140-61661A>G		intron_variant	Intron 1 of 46			ENSP00000507105.1
CACNA1C	ENST00000683781.1	c.140-61661A>G		intron_variant	Intron 1 of 46			ENSP00000507434.1
CACNA1C	ENST00000683840.1	c.140-61661A>G		intron_variant	Intron 1 of 46			ENSP00000507612.1
CACNA1C	ENST00000683956.1	c.140-61661A>G		intron_variant	Intron 1 of 46			ENSP00000506882.1
CACNA1C	ENST00000480911.6	n.1A>G		non_coding_transcript_exon_variant	Exon 1 of 27	5		ENSP00000437936.2

Frequencies

GnomAD3 genomes Cov.: 31

GnomAD4 exome AF: 0.00000138 AC: 2 AN: 1444082 Hom.: 0 Cov.: 32 AF XY: 0.00000279 AC XY: 2 AN XY: 716624

Gnomad4 AFR exome AF: 0.00

Gnomad4 AMR exome AF: 0.00

Gnomad4 ASJ exome AF: 0.00

Gnomad4 EAS exome AF: 0.00

Gnomad4 SAS exome AF: 0.0000121

Gnomad4 FIN exome AF: 0.00

Gnomad4 NFE exome AF: 9.06e-7

Gnomad4 OTH exome AF: 0.00

GnomAD4 genome Cov.: 31

ClinVar

Significance: Uncertain significance

Submissions summary: Uncertain:1

Revision: criteria provided, single submitter

Submissions by phenotype

not provided Uncertain:1

Apr 19, 2021

GeneDx

Significance: Uncertain significance

Review Status: criteria provided, single submitter

Collection Method: clinical testing

Initiation codon variant in a gene for which loss-of-function is not a known mechanism of disease; Not observed in large population cohorts (Lek et al., 2016); Has not been previously published as pathogenic or benign to our knowledge -

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_addAF	Pathogenic	0.45	D
BayesDel_noAF	Pathogenic	0.41
CADD	Benign	20
DANN	Uncertain	0.98
DEOGEN2	Benign	0.016	T;.;.;.;.;.;.;.;.;.;.;.;.;.;.;.;T;.;.;.;.;T;.
Eigen	Benign	-0.040
Eigen_PC	Benign	-0.0037
FATHMM_MKL	Uncertain	0.82	D
M_CAP	Pathogenic	0.93	D
MetaRNN	Pathogenic	0.94	D;D;D;D;D;D;D;D;D;D;D;D;D;D;D;D;D;D;D;D;D;D;D
MetaSVM	Uncertain	0.76	D
PROVEAN	Benign	-0.79	N;N;N;N;N;N;N;N;N;N;N;N;N;N;N;N;N;N;N;N;N;N;N
REVEL	Pathogenic	0.70
Sift	Pathogenic	0.0	D;D;D;D;D;D;D;D;D;D;D;D;D;D;D;D;D;D;D;D;D;D;D
Sift4G	Pathogenic	0.0	D;D;D;D;D;D;D;D;D;D;D;D;D;D;D;D;D;D;D;D;D;D;D
Polyphen		0.22, 0.0020, 0.049, 0.45	.;B;.;B;B;B;B;B;B;B;B;B;B;B;B;B;.;B;B;.;.;.;.
Vest4		0.88
MutPred		0.68		Loss of solvent accessibility (P = 0.0217);Loss of solvent accessibility (P = 0.0217);Loss of solvent accessibility (P = 0.0217);Loss of solvent accessibility (P = 0.0217);Loss of solvent accessibility (P = 0.0217);Loss of solvent accessibility (P = 0.0217);Loss of solvent accessibility (P = 0.0217);Loss of solvent accessibility (P = 0.0217);Loss of solvent accessibility (P = 0.0217);Loss of solvent accessibility (P = 0.0217);Loss of solvent accessibility (P = 0.0217);Loss of solvent accessibility (P = 0.0217);Loss of solvent accessibility (P = 0.0217);Loss of solvent accessibility (P = 0.0217);Loss of solvent accessibility (P = 0.0217);Loss of solvent accessibility (P = 0.0217);Loss of solvent accessibility (P = 0.0217);Loss of solvent accessibility (P = 0.0217);Loss of solvent accessibility (P = 0.0217);Loss of solvent accessibility (P = 0.0217);Loss of solvent accessibility (P = 0.0217);Loss of solvent accessibility (P = 0.0217);Loss of solvent accessibility (P = 0.0217);
MVP		0.99
ClinPred		0.99	D
GERP RS		3.0
gMVP		0.61

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.0		Details are displayed if max score is > 0.2

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Publications

No publications associated with this variant yet.

Other links and lift over

hg19: chr12-2162729;