NM_001330260.2:c.1250A>C

Variant names:

• chr12-51705532-A-C
• rs878854973
• NM_001330260.2:c.1250A>C

Variant summary

Our verdict is Likely pathogenic. Variant got 6 ACMG points: 6P and 0B. PM2 PP2 PP3_Moderate PP5

The NM_001330260.2(SCN8A):​c.1250A>C​(p.Gln417Pro) variant causes a missense change involving the alteration of a conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. In-silico tool predicts a pathogenic outcome for this variant. 12/21 in silico tools predict a damaging outcome for this variant. Variant has been reported in ClinVar as Conflicting classifications of pathogenicity (no stars).

• Frequency: Genomes: not found (cov: 32)
• Consequence: SCN8A NM_001330260.2 missense
• Clinical Significance: Conflicting classifications of pathogenicity criteria provided, conflicting classifications P:1 U:1
• Conservation: PhyloP100: 9.32

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 Likely_pathogenic. Variant got 6 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• PP2: Missense variant in the SCN8A gene, where missense mutations are typically associated with disease (based on misZ statistic). The gene has 213 curated pathogenic missense variants (we use a threshold of 10). The gene has 45 curated benign missense variants. Gene score misZ: 0.78755 (below the threshold of 3.09). Trascript score misZ: 10.436 (above the threshold of 3.09). GenCC associations: The gene is linked to 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.
• PP3: MetaRNN computational evidence supports a deleterious effect, 0.878
• PP5: Variant 12-51705532-A-C is Pathogenic according to our data. Variant chr12-51705532-A-C is described in ClinVar as [Conflicting_classifications_of_pathogenicity]. Clinvar id is 240884.We mark this variant Likely_pathogenic, oryginal submissions are: {Likely_pathogenic=1, Uncertain_significance=1}.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
SCN8A	NM_001330260.2	c.1250A>C	p.Gln417Pro	missense_variant	Exon 10 of 27	ENST00000627620.5	NP_001317189.1
SCN8A	NM_014191.4	c.1250A>C	p.Gln417Pro	missense_variant	Exon 10 of 27	ENST00000354534.11	NP_055006.1
SCN8A	NM_001177984.3	c.1250A>C	p.Gln417Pro	missense_variant	Exon 10 of 26		NP_001171455.1
SCN8A	NM_001369788.1	c.1250A>C	p.Gln417Pro	missense_variant	Exon 10 of 26		NP_001356717.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
SCN8A	ENST00000354534.11	c.1250A>C	p.Gln417Pro	missense_variant	Exon 10 of 27	1	NM_014191.4	ENSP00000346534.4
SCN8A	ENST00000627620.5	c.1250A>C	p.Gln417Pro	missense_variant	Exon 10 of 27	5	NM_001330260.2	ENSP00000487583.2
SCN8A	ENST00000599343.5	c.1250A>C	p.Gln417Pro	missense_variant	Exon 9 of 26	5		ENSP00000476447.3
SCN8A	ENST00000355133.7	c.1250A>C	p.Gln417Pro	missense_variant	Exon 9 of 25	1		ENSP00000347255.4

Frequencies

GnomAD3 genomes Cov.: 32

GnomAD4 exome Cov.: 31

GnomAD4 genome Cov.: 32

ClinVar

Significance: Conflicting classifications of pathogenicity

Submissions summary: Pathogenic:1 Uncertain:1

Revision: criteria provided, conflicting classifications

Submissions by phenotype

Early infantile epileptic encephalopathy with suppression bursts Pathogenic:1

Apr 11, 2017

Labcorp Genetics (formerly Invitae), Labcorp

Significance: Likely pathogenic

Review Status: criteria provided, single submitter

Collection Method: clinical testing

Family studies have indicated that this variant was not present in the parents of an individual with clinical features consistent with an SCN8A-related disease, which suggests that it was de novo in that affected individual. In summary, this variant is a novel missense change that has been observed to occur de novo in an affected individual. This evidence indicates that the variant is pathogenic, but additional data is needed to prove that conclusively. Therefore, this variant has been classified as Likely Pathogenic. Algorithms developed to predict the effect of missense changes on protein structure and function do not agree on the potential impact of this missense change (SIFT: "Deleterious"; PolyPhen-2: "Probably Damaging"; Align-GVGD: "Class C0"). This variant is not present in population databases (ExAC no frequency) and has not been reported in the literature in individuals with a SCN8A-related disease. This sequence change replaces glutamine with proline at codon 417 of the SCN8A protein (p.Gln417Pro). The glutamine residue is highly conserved and there is a moderate physicochemical difference between glutamine and proline. -

Inborn genetic diseases Uncertain:1

Apr 13, 2017

Ambry Genetics

Significance: Uncertain significance

Review Status: criteria provided, single submitter

Collection Method: clinical testing

- -

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Pathogenic	1.0
BayesDel_addAF	Pathogenic	0.52	D
BayesDel_noAF	Pathogenic	0.52
CADD	Pathogenic	27
DANN	Uncertain	1.0
DEOGEN2	Pathogenic	0.98	.;D;.;.;.;.;.
Eigen	Pathogenic	0.84
Eigen_PC	Pathogenic	0.80
FATHMM_MKL	Uncertain	0.96	D
LIST_S2	Uncertain	0.97	D;D;D;.;D;D;D
M_CAP	Pathogenic	0.81	D
MetaRNN	Pathogenic	0.88	D;D;D;D;D;D;D
MetaSVM	Pathogenic	1.1	D
MutationAssessor	Pathogenic	3.1	.;M;M;M;M;M;.
PrimateAI	Pathogenic	0.85	D
PROVEAN	Pathogenic	-5.9	.;D;D;D;.;.;.
REVEL	Pathogenic	0.90
Sift	Pathogenic	0.0	.;D;D;D;.;.;.
Sift4G	Uncertain	0.0030	.;D;D;D;D;D;D
Polyphen		0.97, 1.0	.;D;.;.;D;.;.
Vest4		0.81, 0.81, 0.83, 0.82, 0.79
MutPred		0.33		Gain of glycosylation at Q417 (P = 0.0215);Gain of glycosylation at Q417 (P = 0.0215);Gain of glycosylation at Q417 (P = 0.0215);Gain of glycosylation at Q417 (P = 0.0215);Gain of glycosylation at Q417 (P = 0.0215);Gain of glycosylation at Q417 (P = 0.0215);.;
MVP		0.99
MPC		2.3
ClinPred		1.0	D
GERP RS		5.0
Varity_R		0.98
gMVP		1.0

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: rs878854973; hg19: chr12-52099316;