rs893363

chr3-53813035-G-Achr3-53813035-G-Cchr3-53813035-G-T

Variant summary

Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_000720.4(CACNA1D):c.*1629G>A variant causes a 3 prime UTR change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.554 in 151,888 control chromosomes in the GnomAD database, including 25,373 homozygotes. 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 0.55 (25369 hom., cov: 32)
  • Exomes 𝑓: 0.67 (4 hom.)
• Consequence: CACNA1D NM_000720.4 3_prime_UTR
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.192

Genes affected

CACNA1D (HGNC:1391): (calcium voltage-gated channel subunit alpha1 D) Voltage-dependent calcium channels mediate the entry of calcium ions into excitable cells, and are also involved in a variety of calcium-dependent processes, including muscle contraction, hormone or neurotransmitter release, and gene expression. Calcium channels are multisubunit complexes composed of alpha-1, beta, alpha-2/delta, and gamma subunits. The channel activity is directed by the pore-forming alpha-1 subunit, whereas the others act as auxiliary subunits regulating this activity. The distinctive properties of the calcium channel types are related primarily to the expression of a variety of alpha-1 isoforms, namely alpha-1A, B, C, D, E, and S. This gene encodes the alpha-1D subunit. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2012]

CHDH (HGNC:24288): (choline dehydrogenase) The protein encoded by this gene is a choline dehydrogenase that localizes to the mitochondrion. Variations in this gene can affect susceptibility to choline deficiency. A few transcript variants have been found for this gene, but the full-length nature of only one has been characterized to date. [provided by RefSeq, Dec 2010]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.84).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.939 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
CACNA1D	NM_000720.4	c.*1629G>A		3_prime_UTR_variant	49/49	ENST00000288139.11
CACNA1D	NM_001128840.3	c.*1629G>A		3_prime_UTR_variant	48/48	ENST00000350061.11
CHDH	NM_018397.5	c.*4742C>T		3_prime_UTR_variant	9/9	ENST00000315251.11

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
CACNA1D	ENST00000288139.11	c.*1629G>A		3_prime_UTR_variant	49/49	1	NM_000720.4	P2
CHDH	ENST00000315251.11	c.*4742C>T		3_prime_UTR_variant	9/9	1	NM_018397.5	P1
CACNA1D	ENST00000350061.11	c.*1629G>A		3_prime_UTR_variant	48/48	1	NM_001128840.3

Frequencies

GnomAD3 genomes AF: 0.554 AC: 84046 AN: 151752 Hom.: 25350 Cov.: 32

Gnomad AFR AF: 0.309

Gnomad AMI AF: 0.611

Gnomad AMR AF: 0.683

Gnomad ASJ AF: 0.619

Gnomad EAS AF: 0.962

Gnomad SAS AF: 0.740

Gnomad FIN AF: 0.584

Gnomad MID AF: 0.642

Gnomad NFE AF: 0.619

Gnomad OTH AF: 0.601

GnomAD4 exome AF: 0.667 AC: 12 AN: 18 Hom.: 4 Cov.: 0 AF XY: 0.625 AC XY: 10 AN XY: 16

Gnomad4 AFR exome AF: 0.500

Gnomad4 NFE exome AF: 0.688

GnomAD4 genome AF: 0.554 AC: 84115 AN: 151870 Hom.: 25369 Cov.: 32 AF XY: 0.561 AC XY: 41666 AN XY: 74214

Gnomad4 AFR AF: 0.309

Gnomad4 AMR AF: 0.683

Gnomad4 ASJ AF: 0.619

Gnomad4 EAS AF: 0.962

Gnomad4 SAS AF: 0.740

Gnomad4 FIN AF: 0.584

Gnomad4 NFE AF: 0.619

Gnomad4 OTH AF: 0.606

Alfa AF: 0.604 Hom.: 15683

Bravo AF: 0.549

Asia WGS AF: 0.833 AC: 2893 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.84
Cadd	Benign	0.24
Dann	Benign	0.69
RBP_binding_hub_radar		0.0
RBP_regulation_power_radar		1.2

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

LitVar

Other links and lift over

dbSNP: rs893363; hg19: chr3-53847062; COSMIC: COSV55449332; COSMIC: COSV55449332;