12-51705632-T-G

Position:

• chr12-51705632-T-G

Variant summary

Our verdict is Likely benign. Variant got -4 ACMG points: 0P and 4B. BP4_Strong

The NM_001330260.2(SCN8A):​c.1341+9T>G variant causes a intron 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. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency:
  • Genomes: not found (cov: 32)
  • Exomes 𝑓: 0.0011 (0 hom.)
  • Failed GnomAD Quality Control
• Consequence: SCN8A NM_001330260.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.114

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]

SCN8A (HGNC:):

ACMG classification

Verdict is Likely_benign. Variant got -4 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.72).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
SCN8A	NM_001330260.2	c.1341+9T>G		intron_variant		ENST00000627620.5	NP_001317189.1
SCN8A	NM_014191.4	c.1341+9T>G		intron_variant		ENST00000354534.11	NP_055006.1
SCN8A	NM_001177984.3	c.1341+9T>G		intron_variant			NP_001171455.1
SCN8A	NM_001369788.1	c.1341+9T>G		intron_variant			NP_001356717.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
SCN8A	ENST00000354534.11	c.1341+9T>G		intron_variant		1	NM_014191.4	ENSP00000346534.4
SCN8A	ENST00000627620.5	c.1341+9T>G		intron_variant		5	NM_001330260.2	ENSP00000487583.2
SCN8A	ENST00000599343.5	c.1341+9T>G		intron_variant		5		ENSP00000476447.3
SCN8A	ENST00000355133.7	c.1341+9T>G		intron_variant		1		ENSP00000347255.4

Frequencies

GnomAD3 genomes Cov.: 32

GnomAD4 exome Data not reliable, filtered out with message: AS_VQSR AF: 0.00113 AC: 1639 AN: 1453446 Hom.: 0 Cov.: 31 AF XY: 0.00107 AC XY: 770 AN XY: 722596

Gnomad4 AFR exome AF: 0.000720

Gnomad4 AMR exome AF: 0.0000227

Gnomad4 ASJ exome AF: 0.000385

Gnomad4 EAS exome AF: 0.000126

Gnomad4 SAS exome AF: 0.000446

Gnomad4 FIN exome AF: 0.00

Gnomad4 NFE exome AF: 0.00136

Gnomad4 OTH exome AF: 0.000915

GnomAD4 genome Cov.: 32

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.72
CADD	Benign	13
DANN	Benign	0.80

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.18		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: rs373377688; hg19: chr12-52099416;