12-51591343-TCGC-T

Position:

• chr12-51591343-TCGC-T

Variant summary

Our verdict is Uncertain significance. Variant got 1 ACMG points: 2P and 1B. PM2 BP6

The NM_001330260.2(SCN8A):​c.-61_-59delCGC variant causes a 5 prime UTR change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.000281 in 3,554 control chromosomes in the GnomAD database, with no homozygous occurrence. Variant has been reported in ClinVar as Likely benign (no stars).

• Frequency:
  • Genomes: not found (cov: 30)
  • Exomes 𝑓: 0.00028 (0 hom.)
• Consequence: SCN8A NM_001330260.2 5_prime_UTR
• Clinical Significance: Likely benign no assertion criteria provided B:1
• Conservation: PhyloP100: 0.597

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
• BP6: Variant 12-51591343-TCGC-T is Benign according to our data. Variant chr12-51591343-TCGC-T is described in ClinVar as [Likely_benign]. Clinvar id is 3029905.Status of the report is no_assertion_criteria_provided, 0 stars.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
SCN8A	NM_001330260.2	c.-61_-59delCGC		5_prime_UTR_variant	1/27	ENST00000627620.5	NP_001317189.1
SCN8A	NM_014191.4	c.-61_-59delCGC		5_prime_UTR_variant	1/27	ENST00000354534.11	NP_055006.1
SCN8A	NM_001177984.3	c.-61_-59delCGC		5_prime_UTR_variant	1/26		NP_001171455.1
SCN8A	NM_001369788.1	c.-61_-59delCGC		5_prime_UTR_variant	1/26		NP_001356717.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
SCN8A	ENST00000354534	c.-61_-59delCGC		5_prime_UTR_variant	1/27	1	NM_014191.4	ENSP00000346534.4
SCN8A	ENST00000627620	c.-61_-59delCGC		5_prime_UTR_variant	1/27	5	NM_001330260.2	ENSP00000487583.2

Frequencies

GnomAD3 genomes Cov.: 30

GnomAD4 exome AF: 0.000281 AC: 1 AN: 3554 Hom.: 0 AF XY: 0.000398 AC XY: 1 AN XY: 2512

Gnomad4 AFR exome AF: 0.00

Gnomad4 AMR exome AF: 0.00

Gnomad4 ASJ exome AF: 0.00

Gnomad4 EAS exome AF: 0.00

Gnomad4 SAS exome AF: 0.00

Gnomad4 FIN exome AF: 0.00

Gnomad4 NFE exome AF: 0.00

Gnomad4 OTH exome AF: 0.00725

GnomAD4 genome Cov.: 30

ClinVar

Significance: Likely benign

Submissions summary: Benign:1

Revision: no assertion criteria provided

Submissions by phenotype

SCN8A-related disorder Benign:1

Likely benign, no assertion criteria provided

clinical testing

PreventionGenetics, part of Exact Sciences

Apr 19, 2021

This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications). -

Computational scores

Source: dbNSFP v4.3

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: rs1939211278; hg19: chr12-51985127;