12-51662864-C-T

Position:

• chr12-51662864-C-T

Variant summary

Our verdict is Uncertain significance. Variant got 1 ACMG points: 3P and 2B. PM2 PP2 BP4_Moderate

The NM_001330260.2(SCN8A):​c.47C>T​(p.Pro16Leu) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. In-silico tool predicts a benign outcome for this variant. 12/21 in silico tools predict a benign outcome for this variant. Variant has been reported in ClinVar as Uncertain significance (★).

• Frequency: Genomes: not found (cov: 32)
• Consequence: SCN8A NM_001330260.2 missense
• Clinical Significance: Uncertain significance criteria provided, single submitter U:1
• Conservation: PhyloP100: 1.44

Genes affected

SCN8A (HGNC:10596): (sodium voltage-gated channel alpha subunit 8) This gene encodes a member of the sodium channel alpha subunit gene family. The encoded protein forms the ion pore region of the voltage-gated sodium channel. This protein is essential for the rapid membrane depolarization that occurs during the formation of the action potential in excitable neurons. Mutations in this gene are associated with cognitive disability, pancerebellar atrophy and ataxia. Alternate splicing results in multiple transcript variants.[provided by RefSeq, May 2010]

ACMG classification

Verdict is Uncertain_significance. Variant got 1 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• PP2: Missense variant in gene, where missense usually causes diseases (based on misZ statistic), SCN8A. . Gene score misZ: 0.78755 (greater than the threshold 3.09). Trascript score misZ: 10.436 (greater than threshold 3.09). The gene has 213 curated pathogenic missense variants (we use a threshold of 10). The gene has 45 curated benign missense variants. GenCC has associacion of the gene with myoclonus, familial, 2, infantile convulsions and choreoathetosis, cognitive impairment with or without cerebellar ataxia, undetermined early-onset epileptic encephalopathy, complex neurodevelopmental disorder, developmental and epileptic encephalopathy, 13, benign familial infantile epilepsy, seizures, benign familial infantile, 5.
• BP4: Computational evidence support a benign effect (MetaRNN=0.13262832).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
SCN8A	NM_001330260.2	c.47C>T	p.Pro16Leu	missense_variant	2/27	ENST00000627620.5	NP_001317189.1
SCN8A	NM_014191.4	c.47C>T	p.Pro16Leu	missense_variant	2/27	ENST00000354534.11	NP_055006.1
SCN8A	NM_001177984.3	c.47C>T	p.Pro16Leu	missense_variant	2/26		NP_001171455.1
SCN8A	NM_001369788.1	c.47C>T	p.Pro16Leu	missense_variant	2/26		NP_001356717.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
SCN8A	ENST00000354534.11	c.47C>T	p.Pro16Leu	missense_variant	2/27	1	NM_014191.4	ENSP00000346534.4
SCN8A	ENST00000627620.5	c.47C>T	p.Pro16Leu	missense_variant	2/27	5	NM_001330260.2	ENSP00000487583.2
SCN8A	ENST00000599343.5	c.47C>T	p.Pro16Leu	missense_variant	1/26	5		ENSP00000476447.3
SCN8A	ENST00000355133.7	c.47C>T	p.Pro16Leu	missense_variant	1/25	1		ENSP00000347255.4

Frequencies

GnomAD3 genomes Cov.: 32

GnomAD4 exome Cov.: 31

GnomAD4 genome Cov.: 32

ClinVar

Significance: Uncertain significance

Submissions summary: Uncertain:1

Revision: criteria provided, single submitter

Submissions by phenotype

Early infantile epileptic encephalopathy with suppression bursts Uncertain:1

Uncertain significance, criteria provided, single submitter

clinical testing

Labcorp Genetics (formerly Invitae), Labcorp

Feb 04, 2022

This variant is not present in population databases (gnomAD no frequency). This sequence change replaces proline, which is neutral and non-polar, with leucine, which is neutral and non-polar, at codon 16 of the SCN8A protein (p.Pro16Leu). This variant has not been reported in the literature in individuals affected with SCN8A-related conditions. In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. Algorithms developed to predict the effect of missense changes on protein structure and function are either unavailable or do not agree on the potential impact of this missense change (SIFT: "Deleterious"; PolyPhen-2: "Benign"; Align-GVGD: "Class C0"). ClinVar contains an entry for this variant (Variation ID: 850466). -

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.10
BayesDel_addAF	Uncertain	0.088	D
BayesDel_noAF	Benign	-0.11
CADD	Uncertain	26
DANN	Benign	0.86
DEOGEN2	Benign	0.31	.;T;.;.;.;.
Eigen	Benign	-0.093
Eigen_PC	Benign	0.067
FATHMM_MKL	Uncertain	0.78	D
LIST_S2	Uncertain	0.93	D;D;D;.;D;D
M_CAP	Benign	0.040	D
MetaRNN	Benign	0.13	T;T;T;T;T;T
MetaSVM	Uncertain	0.35	D
MutationAssessor	Benign	1.8	.;L;L;L;L;L
PrimateAI	Uncertain	0.64	T
PROVEAN	Benign	-0.44	.;N;N;N;.;.
REVEL	Uncertain	0.30
Sift	Benign	0.70	.;T;T;T;.;.
Sift4G	Benign	0.54	.;T;T;T;T;T
Polyphen		0.085	.;B;.;.;.;.
Vest4		0.26, 0.39, 0.38, 0.37, 0.39
MutPred		0.32		Loss of glycosylation at S13 (P = 0.1317);Loss of glycosylation at S13 (P = 0.1317);Loss of glycosylation at S13 (P = 0.1317);Loss of glycosylation at S13 (P = 0.1317);Loss of glycosylation at S13 (P = 0.1317);Loss of glycosylation at S13 (P = 0.1317);
MVP		0.67
MPC		0.95
ClinPred		0.19	T
GERP RS		5.0
Varity_R		0.14
gMVP		0.79

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: rs1940950901; hg19: chr12-52056648;