2-166086767-T-G

Variant names:

• chr2-166086767-T-G
• rs11890028
• NM_001165963.4:c.-141-8966A>C

Variant summary

Our verdict is Benign. The variant received -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_001165963.4(SCN1A):​c.-141-8966A>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.245 in 152,130 control chromosomes in the GnomAD database, including 4,812 homozygotes. 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: 𝑓 0.25 (4812 hom., cov: 31)
• Consequence: SCN1A NM_001165963.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.159
• Publications: 21 publications found

Genes affected

SCN1A (HGNC:10585): (sodium voltage-gated channel alpha subunit 1) Voltage-dependent sodium channels are heteromeric complexes that regulate sodium exchange between intracellular and extracellular spaces and are essential for the generation and propagation of action potentials in muscle cells and neurons. Each sodium channel is composed of a large pore-forming, glycosylated alpha subunit and two smaller beta subunits. This gene encodes a sodium channel alpha subunit, which has four homologous domains, each of which contains six transmembrane regions. Allelic variants of this gene are associated with generalized epilepsy with febrile seizures and epileptic encephalopathy. Alternative splicing results in multiple transcript variants. The RefSeq Project has decided to create four representative RefSeq records. Three of the transcript variants are supported by experimental evidence and the fourth contains alternate 5' untranslated exons, the exact combination of which have not been experimentally confirmed for the full-length transcript. [provided by RefSeq, Oct 2015]

SCN1A-AS1 (HGNC:54069): (SCN1A and SCN9A antisense RNA 1)

ACMG classification

Our verdict: Benign. The variant received -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.9).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.286 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001165963.4. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	SCN1A	NM_001165963.4	MANE Select	c.-141-8966A>C		intron	N/A	NP_001159435.1
	SCN1A	NM_001202435.3		c.-141-8966A>C		intron	N/A	NP_001189364.1
	SCN1A	NM_001353948.2		c.-49-13097A>C		intron	N/A	NP_001340877.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	SCN1A	ENST00000674923.1	MANE Select	c.-141-8966A>C		intron	N/A	ENSP00000501589.1
	SCN1A	ENST00000303395.9	TSL:5	c.-141-8966A>C		intron	N/A	ENSP00000303540.4
	SCN1A	ENST00000409050.2	TSL:5	c.-187-8920A>C		intron	N/A	ENSP00000386312.1

Frequencies

GnomAD3 genomes AF: 0.245 AC: 37290 AN: 152012 Hom.: 4819 Cov.: 31

Gnomad AFR AF: 0.181

Gnomad AMI AF: 0.299

Gnomad AMR AF: 0.232

Gnomad ASJ AF: 0.393

Gnomad EAS AF: 0.125

Gnomad SAS AF: 0.298

Gnomad FIN AF: 0.228

Gnomad MID AF: 0.513

Gnomad NFE AF: 0.285

Gnomad OTH AF: 0.284

We have no GnomAD4 exomes data on this position. Probably position not covered by the project.

GnomAD4 genome AF: 0.245 AC: 37293 AN: 152130 Hom.: 4812 Cov.: 31 AF XY: 0.243 AC XY: 18066 AN XY: 74368

African (AFR) AF: 0.181 AC: 7522 AN: 41532

American (AMR) AF: 0.231 AC: 3533 AN: 15276

Ashkenazi Jewish (ASJ) AF: 0.393 AC: 1363 AN: 3470

East Asian (EAS) AF: 0.124 AC: 642 AN: 5168

South Asian (SAS) AF: 0.298 AC: 1439 AN: 4822

European-Finnish (FIN) AF: 0.228 AC: 2416 AN: 10580

Middle Eastern (MID) AF: 0.507 AC: 148 AN: 292

European-Non Finnish (NFE) AF: 0.285 AC: 19362 AN: 67972

Other (OTH) AF: 0.283 AC: 596 AN: 2108

Alfa AF: 0.272 Hom.: 18851

Bravo AF: 0.243

Asia WGS AF: 0.212 AC: 739 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.90
CADD	Benign	2.4
DANN	Benign	0.55
PhyloP100		-0.16

Splicing

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Other links and lift over

dbSNP: rs11890028; hg19: chr2-166943277;