rs2239128

Variant names:

Your query was ambiguous. Multiple possible variants found:

Variant summary

Our verdict is Likely benign. The variant received -4 ACMG points: 0P and 4B. BP4_Strong

The NM_000719.7(CACNA1C):c.3945+96T>A variant causes a intron change involving the alteration of a non-conserved nucleotide. In-silico tool predicts a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

Frequency

Genomes: 𝑓 0.0 ( 0 hom., cov: 29)

Exomes 𝑓: 0.0 ( 0 hom. )

Failed GnomAD Quality Control

Consequence

CACNA1C
NM_000719.7 intron

Scores

Clinical Significance

Not reported in ClinVar

Conservation

PhyloP100: -0.00500

Publications

10 publications found

Variant links:

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]

CACNA1C Gene-Disease associations (from GenCC):

Timothy syndrome
Inheritance: AD Classification: DEFINITIVE, STRONG, SUPPORTIVE Submitted by: Ambry Genetics, Orphanet, G2P, Labcorp Genetics (formerly Invitae)
neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures
Inheritance: AD Classification: STRONG Submitted by: Ambry Genetics
long QT syndrome
Inheritance: AD Classification: MODERATE Submitted by: ClinGen
long QT syndrome 8
Inheritance: AD Classification: MODERATE Submitted by: Ambry Genetics
Brugada syndrome
Inheritance: AD Classification: SUPPORTIVE, NO_KNOWN Submitted by: Orphanet, ClinGen
Brugada syndrome 3
Inheritance: AD Classification: LIMITED, NO_KNOWN Submitted by: Ambry Genetics, Genomics England PanelApp, Labcorp Genetics (formerly Invitae)
intellectual disability
Inheritance: AD Classification: LIMITED Submitted by: Ambry Genetics
short QT syndrome
Inheritance: AD Classification: LIMITED, NO_KNOWN Submitted by: Ambry Genetics, ClinGen

CACNA1C links:

Genome browser will be placed here

ACMG classification

Classification was made for transcript

Our verdict: Likely_benign. The variant received -4 ACMG points.

BP4

Computational evidence support a benign effect (BayesDel_noAF=-0.83).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
CACNA1C	NM_000719.7 link	c.3945+96T>A		intron_variant	Intron 31 of 46	ENST00000399655.6	NP_000710.5
CACNA1C	NM_001167623.2 link	c.3945+96T>A		intron_variant	Intron 31 of 46	ENST00000399603.6	NP_001161095.1

Ensembl

Gene	Transcript	HGVSc	Effect	Exon rank	TSL	MANE	Protein
CACNA1C	ENST00000399603.6 link	c.3945+96T>A	intron_variant	Intron 31 of 46	5	NM_001167623.2	ENSP00000382512.1
CACNA1C	ENST00000399655.6 link	c.3945+96T>A	intron_variant	Intron 31 of 46	1	NM_000719.7	ENSP00000382563.1
CACNA1C	ENST00000682544.1 link	c.4179+96T>A	intron_variant	Intron 33 of 49			ENSP00000507184.1
CACNA1C	ENST00000406454.8 link	c.3945+96T>A	intron_variant	Intron 31 of 47	5		ENSP00000385896.3
CACNA1C	ENST00000399634.6 link	c.3913-3037T>A	intron_variant	Intron 30 of 46	5		ENSP00000382542.2
CACNA1C	ENST00000683824.1 link	c.4110+96T>A	intron_variant	Intron 32 of 47			ENSP00000507867.1
CACNA1C	ENST00000347598.9 link	c.4089+96T>A	intron_variant	Intron 33 of 48	1		ENSP00000266376.6
CACNA1C	ENST00000344100.7 link	c.3945+96T>A	intron_variant	Intron 31 of 46	1		ENSP00000341092.3
CACNA1C	ENST00000327702.12 link	c.3945+96T>A	intron_variant	Intron 31 of 47	1		ENSP00000329877.7
CACNA1C	ENST00000399617.6 link	c.3945+96T>A	intron_variant	Intron 31 of 47	5		ENSP00000382526.1
CACNA1C	ENST00000682462.1 link	c.4035+96T>A	intron_variant	Intron 31 of 46			ENSP00000507105.1
CACNA1C	ENST00000683781.1 link	c.4035+96T>A	intron_variant	Intron 31 of 46			ENSP00000507434.1
CACNA1C	ENST00000683840.1 link	c.4035+96T>A	intron_variant	Intron 31 of 46			ENSP00000507612.1
CACNA1C	ENST00000683956.1 link	c.4035+96T>A	intron_variant	Intron 31 of 46			ENSP00000506882.1
CACNA1C	ENST00000399638.5 link	c.4029+96T>A	intron_variant	Intron 32 of 47	1		ENSP00000382547.1
CACNA1C	ENST00000335762.10 link	c.4020+96T>A	intron_variant	Intron 32 of 47	5		ENSP00000336982.5
CACNA1C	ENST00000399606.5 link	c.4005+96T>A	intron_variant	Intron 32 of 47	1		ENSP00000382515.1
CACNA1C	ENST00000399621.5 link	c.3945+96T>A	intron_variant	Intron 31 of 46	1		ENSP00000382530.1
CACNA1C	ENST00000399637.5 link	c.3945+96T>A	intron_variant	Intron 31 of 46	1		ENSP00000382546.1
CACNA1C	ENST00000402845.7 link	c.3945+96T>A	intron_variant	Intron 31 of 46	1		ENSP00000385724.3
CACNA1C	ENST00000399629.5 link	c.3997-3037T>A	intron_variant	Intron 31 of 46	1		ENSP00000382537.1
CACNA1C	ENST00000682336.1 link	c.3988-3037T>A	intron_variant	Intron 31 of 46			ENSP00000507898.1
CACNA1C	ENST00000399591.5 link	c.3913-3037T>A	intron_variant	Intron 30 of 45	1		ENSP00000382500.1
CACNA1C	ENST00000399595.5 link	c.3913-3037T>A	intron_variant	Intron 30 of 45	1		ENSP00000382504.1
CACNA1C	ENST00000399649.5 link	c.3907-3037T>A	intron_variant	Intron 30 of 45	1		ENSP00000382557.1
CACNA1C	ENST00000399597.5 link	c.3945+96T>A	intron_variant	Intron 31 of 46	1		ENSP00000382506.1
CACNA1C	ENST00000399601.5 link	c.3945+96T>A	intron_variant	Intron 31 of 46	1		ENSP00000382510.1
CACNA1C	ENST00000399641.6 link	c.3945+96T>A	intron_variant	Intron 31 of 46	1		ENSP00000382549.1
CACNA1C	ENST00000399644.5 link	c.3945+96T>A	intron_variant	Intron 31 of 46	1		ENSP00000382552.1
CACNA1C	ENST00000682835.1 link	c.3945+96T>A	intron_variant	Intron 31 of 46			ENSP00000507282.1
CACNA1C	ENST00000683482.1 link	c.3936+96T>A	intron_variant	Intron 31 of 46			ENSP00000507169.1
CACNA1C	ENST00000682686.1 link	c.3913-3037T>A	intron_variant	Intron 30 of 45			ENSP00000507309.1

Frequencies

GnomAD3 genomes

AF:

0.00

AC:

AN:

151412

Hom.:

Cov.:

Gnomad AFR

AF:

0.00

Gnomad AMI

AF:

0.00

Gnomad AMR

AF:

0.00

Gnomad ASJ

AF:

0.00

Gnomad EAS

AF:

0.00

Gnomad SAS

AF:

0.00

Gnomad FIN

AF:

0.00

Gnomad MID

AF:

0.00

Gnomad NFE

AF:

0.00

Gnomad OTH

AF:

0.00

GnomAD4 exome

Data not reliable, filtered out with message: AC0

AF:

0.00

AC:

AN:

923346

Hom.:

AF XY:

0.00

AC XY:

AN XY:

480818

African (AFR)

AF:

0.00

AC:

AN:

23216

American (AMR)

AF:

0.00

AC:

AN:

43342

Ashkenazi Jewish (ASJ)

AF:

0.00

AC:

AN:

22338

East Asian (EAS)

AF:

0.00

AC:

AN:

37122

South Asian (SAS)

AF:

0.00

AC:

AN:

74430

European-Finnish (FIN)

AF:

0.00

AC:

AN:

51544

Middle Eastern (MID)

AF:

0.00

AC:

AN:

4344

European-Non Finnish (NFE)

AF:

0.00

AC:

AN:

624438

Other (OTH)

AF:

0.00

AC:

AN:

42572

GnomAD4 genome

Data not reliable, filtered out with message: AC0

AF:

0.00

AC:

AN:

151412

Hom.:

Cov.:

AF XY:

0.00

AC XY:

AN XY:

73880

African (AFR)

AF:

0.00

AC:

AN:

41076

American (AMR)

AF:

0.00

AC:

AN:

15240

Ashkenazi Jewish (ASJ)

AF:

0.00

AC:

AN:

3462

East Asian (EAS)

AF:

0.00

AC:

AN:

5118

South Asian (SAS)

AF:

0.00

AC:

AN:

4786

European-Finnish (FIN)

AF:

0.00

AC:

AN:

10496

Middle Eastern (MID)

AF:

0.00

AC:

AN:

314

European-Non Finnish (NFE)

AF:

0.00

AC:

AN:

67932

Other (OTH)

AF:

0.00

AC:

AN:

2078

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name

Calibrated prediction

Score

Prediction

BayesDel_noAF

Benign

-0.83

CADD

Benign

0.20

(source)

DANN

Benign

0.57

PhyloP100

-0.0050

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

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Variant summary

Frequency

Consequence

Scores

Clinical Significance

Conservation

Publications

ACMG classification

Transcripts

RefSeq

Ensembl

Frequencies

ClinVar

Computational scores

Splicing

Publications

Other links and lift over