chr10-18427216-T-C

Variant names:

• chr10-18427216-T-C
• rs10741058
• NM_201596.3:c.333+25173T>C

Variant summary

Our verdict is Benign. The variant received -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_201596.3(CACNB2):​c.333+25173T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.88 in 152,146 control chromosomes in the GnomAD database, including 59,101 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 0.88 (59101 hom., cov: 31)
• Consequence: CACNB2 NM_201596.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.142
• Publications: 4 publications found

Genes affected

CACNB2 (HGNC:1402): (calcium voltage-gated channel auxiliary subunit beta 2) This gene encodes a subunit of a voltage-dependent calcium channel protein that is a member of the voltage-gated calcium channel superfamily. The gene product was originally identified as an antigen target in Lambert-Eaton myasthenic syndrome, an autoimmune disorder. Mutations in this gene are associated with Brugada syndrome. Alternatively spliced variants encoding different isoforms have been described. [provided by RefSeq, Feb 2013]

CACNB2 Gene-Disease associations (from GenCC):

• Brugada syndrome 4

  Inheritance: AD, Unknown Classification: LIMITED, NO_KNOWN Submitted by: Labcorp Genetics (formerly Invitae), Genomics England PanelApp, Ambry Genetics, Laboratory for Molecular Medicine
• Brugada syndrome 1

  Inheritance: AD Classification: NO_KNOWN Submitted by: ClinGen
• hypertrophic cardiomyopathy

  Inheritance: AD Classification: NO_KNOWN Submitted by: ClinGen
• short QT syndrome

  Inheritance: AD Classification: NO_KNOWN Submitted by: ClinGen

ACMG classification

Our verdict: Benign. The variant received -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-1.01).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.936 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
CACNB2	NM_201596.3	c.333+25173T>C		intron_variant	Intron 3 of 13	ENST00000324631.13	NP_963890.2
CACNB2	NM_201590.3	c.171+25173T>C		intron_variant	Intron 2 of 12	ENST00000377329.10	NP_963884.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
CACNB2	ENST00000324631.13	c.333+25173T>C		intron_variant	Intron 3 of 13	1	NM_201596.3	ENSP00000320025.8
CACNB2	ENST00000377329.10	c.171+25173T>C		intron_variant	Intron 2 of 12	1	NM_201590.3	ENSP00000366546.4

Frequencies

GnomAD3 genomes AF: 0.880 AC: 133754 AN: 152028 Hom.: 59062 Cov.: 31

Gnomad AFR AF: 0.927

Gnomad AMI AF: 0.880

Gnomad AMR AF: 0.773

Gnomad ASJ AF: 0.951

Gnomad EAS AF: 0.958

Gnomad SAS AF: 0.897

Gnomad FIN AF: 0.838

Gnomad MID AF: 0.905

Gnomad NFE AF: 0.870

Gnomad OTH AF: 0.888

We have no GnomAD4 exomes data on this position. Probably position not covered by the project.

GnomAD4 genome AF: 0.880 AC: 133846 AN: 152146 Hom.: 59101 Cov.: 31 AF XY: 0.876 AC XY: 65141 AN XY: 74358

African (AFR) AF: 0.927 AC: 38491 AN: 41518

American (AMR) AF: 0.773 AC: 11806 AN: 15282

Ashkenazi Jewish (ASJ) AF: 0.951 AC: 3299 AN: 3470

East Asian (EAS) AF: 0.958 AC: 4955 AN: 5172

South Asian (SAS) AF: 0.897 AC: 4318 AN: 4812

European-Finnish (FIN) AF: 0.838 AC: 8867 AN: 10578

Middle Eastern (MID) AF: 0.905 AC: 266 AN: 294

European-Non Finnish (NFE) AF: 0.870 AC: 59165 AN: 67998

Other (OTH) AF: 0.889 AC: 1878 AN: 2112

Alfa AF: 0.874 Hom.: 79061

Bravo AF: 0.876

Asia WGS AF: 0.933 AC: 3245 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-1.0
CADD	Benign	2.0
DANN	Benign	0.44
PhyloP100		-0.14
Mutation Taster		=100/0	polymorphism (auto)

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

Other links and lift over

dbSNP: rs10741058; hg19: chr10-18716145;