rs7535696

Positions:

• chr1-196402302-T-C

Variant summary

Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_198503.5(KCNT2):​c.1186-3631A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.271 in 151,442 control chromosomes in the GnomAD database, including 5,953 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 0.27 (5953 hom., cov: 32)
• Consequence: KCNT2 NM_198503.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.0780

Genes affected

KCNT2 (HGNC:18866): (potassium sodium-activated channel subfamily T member 2) Enables chloride-activated potassium channel activity. Involved in potassium ion export across plasma membrane. Located in plasma membrane. Implicated in developmental and epileptic encephalopathy 57. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.92).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.325 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
KCNT2	NM_198503.5	c.1186-3631A>G		intron_variant		ENST00000294725.14

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
KCNT2	ENST00000294725.14	c.1186-3631A>G		intron_variant		1	NM_198503.5	P4

Frequencies

GnomAD3 genomes AF: 0.271 AC: 40981 AN: 151328 Hom.: 5951 Cov.: 32

Gnomad AFR AF: 0.153

Gnomad AMI AF: 0.375

Gnomad AMR AF: 0.332

Gnomad ASJ AF: 0.351

Gnomad EAS AF: 0.335

Gnomad SAS AF: 0.310

Gnomad FIN AF: 0.347

Gnomad MID AF: 0.247

Gnomad NFE AF: 0.304

Gnomad OTH AF: 0.277

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

GnomAD4 genome AF: 0.271 AC: 40988 AN: 151442 Hom.: 5953 Cov.: 32 AF XY: 0.276 AC XY: 20436 AN XY: 73942

Gnomad4 AFR AF: 0.153

Gnomad4 AMR AF: 0.332

Gnomad4 ASJ AF: 0.351

Gnomad4 EAS AF: 0.335

Gnomad4 SAS AF: 0.311

Gnomad4 FIN AF: 0.347

Gnomad4 NFE AF: 0.304

Gnomad4 OTH AF: 0.276

Alfa AF: 0.289 Hom.: 2375

Bravo AF: 0.262

Asia WGS AF: 0.313 AC: 1070 AN: 3426

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.92
CADD	Benign	2.1
DANN	Benign	0.54

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: rs7535696; hg19: chr1-196371432;