rs879255698

Variant names:

• chr12-51705503-G-C
• rs879255698
• NM_001330260.2:c.1221G>C

Variant summary

Our verdict is Uncertain significance. Variant got 5 ACMG points: 5P and 0B. PM2 PP2 PP3_Moderate

The NM_001330260.2(SCN8A):​c.1221G>C​(p.Leu407Phe) variant causes a missense change. The variant was absent in control chromosomes in GnomAD project. In-silico tool predicts a pathogenic outcome for this variant. Variant has been reported in ClinVar as not provided (no stars).

• Frequency: Genomes: not found (cov: 32)
• Consequence: SCN8A NM_001330260.2 missense
• Clinical Significance: not provided no classification provided O:1
• Conservation: PhyloP100: 6.91

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 5 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, 0.928

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
SCN8A	NM_001330260.2	c.1221G>C	p.Leu407Phe	missense_variant	Exon 10 of 27	ENST00000627620.5	NP_001317189.1
SCN8A	NM_014191.4	c.1221G>C	p.Leu407Phe	missense_variant	Exon 10 of 27	ENST00000354534.11	NP_055006.1
SCN8A	NM_001177984.3	c.1221G>C	p.Leu407Phe	missense_variant	Exon 10 of 26		NP_001171455.1
SCN8A	NM_001369788.1	c.1221G>C	p.Leu407Phe	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.1221G>C	p.Leu407Phe	missense_variant	Exon 10 of 27	1	NM_014191.4	ENSP00000346534.4
SCN8A	ENST00000627620.5	c.1221G>C	p.Leu407Phe	missense_variant	Exon 10 of 27	5	NM_001330260.2	ENSP00000487583.2
SCN8A	ENST00000599343.5	c.1221G>C	p.Leu407Phe	missense_variant	Exon 9 of 26	5		ENSP00000476447.3
SCN8A	ENST00000355133.7	c.1221G>C	p.Leu407Phe	missense_variant	Exon 9 of 25	1		ENSP00000347255.4

Frequencies

GnomAD3 genomes Cov.: 32

GnomAD4 exome Cov.: 32

GnomAD4 genome Cov.: 32

ClinVar

Significance: not provided

Submissions summary: Other:1

Revision: no classification provided

Submissions by phenotype

Developmental and epileptic encephalopathy, 13 Other:1

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GeneReviews

Significance: not provided

Review Status: no classification provided

Collection Method: literature only

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Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Pathogenic	0.98
BayesDel_addAF	Pathogenic	0.57	D
BayesDel_noAF	Pathogenic	0.59
CADD	Uncertain	25
DANN	Uncertain	1.0
DEOGEN2	Pathogenic	0.99	.;D;.;.;.;.;.
Eigen	Pathogenic	0.83
Eigen_PC	Pathogenic	0.72
FATHMM_MKL	Uncertain	0.93	D
LIST_S2	Pathogenic	0.99	D;D;D;.;D;D;D
M_CAP	Pathogenic	0.88	D
MetaRNN	Pathogenic	0.93	D;D;D;D;D;D;D
MetaSVM	Pathogenic	1.1	D
MutationAssessor	Pathogenic	3.9	.;H;H;H;H;H;.
PrimateAI	Pathogenic	0.88	D
PROVEAN	Uncertain	-3.9	.;D;D;D;.;.;.
REVEL	Pathogenic	0.97
Sift	Uncertain	0.0010	.;D;D;D;.;.;.
Sift4G	Uncertain	0.012	.;D;D;D;D;D;D
Polyphen		1.0	.;D;.;.;D;.;.
Vest4		0.89, 0.91, 0.91, 0.89
MutPred		0.68		Gain of catalytic residue at A408 (P = 0.2423);Gain of catalytic residue at A408 (P = 0.2423);Gain of catalytic residue at A408 (P = 0.2423);Gain of catalytic residue at A408 (P = 0.2423);Gain of catalytic residue at A408 (P = 0.2423);Gain of catalytic residue at A408 (P = 0.2423);.;
MVP		0.97
MPC		2.2
ClinPred		1.0	D
GERP RS		4.1
Varity_R		0.91
gMVP		0.99

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: rs879255698; hg19: chr12-52099287;