rs10801533

Variant names:

• chr1-196426741-G-A
• rs10801533
• NM_198503.5:c.985-753C>T

Your query was ambiguous. Multiple possible variants found:

• chr1-196426741-G-A
• chr1-196426741-G-T

Variant summary

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

The NM_198503.5(KCNT2):​c.985-753C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.542 in 151,124 control chromosomes in the GnomAD database, including 22,899 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 0.54 (22899 hom., cov: 29)
• Consequence: KCNT2 NM_198503.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.487
• Publications: 2 publications found

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]

KCNT2 Gene-Disease associations (from GenCC):

• developmental and epileptic encephalopathy, 57

  Inheritance: AD Classification: STRONG, MODERATE, LIMITED Submitted by: G2P, Ambry Genetics, Labcorp Genetics (formerly Invitae)

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.89).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.655 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
KCNT2	NM_198503.5	c.985-753C>T		intron_variant	Intron 10 of 27	ENST00000294725.14	NP_940905.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
KCNT2	ENST00000294725.14	c.985-753C>T		intron_variant	Intron 10 of 27	1	NM_198503.5	ENSP00000294725.8

Frequencies

GnomAD3 genomes AF: 0.543 AC: 81931 AN: 151006 Hom.: 22884 Cov.: 29

Gnomad AFR AF: 0.388

Gnomad AMI AF: 0.624

Gnomad AMR AF: 0.572

Gnomad ASJ AF: 0.613

Gnomad EAS AF: 0.650

Gnomad SAS AF: 0.675

Gnomad FIN AF: 0.516

Gnomad MID AF: 0.709

Gnomad NFE AF: 0.609

Gnomad OTH AF: 0.577

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

GnomAD4 genome AF: 0.542 AC: 81984 AN: 151124 Hom.: 22899 Cov.: 29 AF XY: 0.541 AC XY: 39874 AN XY: 73742

African (AFR) AF: 0.389 AC: 15983 AN: 41126

American (AMR) AF: 0.572 AC: 8641 AN: 15108

Ashkenazi Jewish (ASJ) AF: 0.613 AC: 2125 AN: 3468

East Asian (EAS) AF: 0.649 AC: 3315 AN: 5104

South Asian (SAS) AF: 0.675 AC: 3217 AN: 4768

European-Finnish (FIN) AF: 0.516 AC: 5396 AN: 10448

Middle Eastern (MID) AF: 0.728 AC: 214 AN: 294

European-Non Finnish (NFE) AF: 0.609 AC: 41305 AN: 67794

Other (OTH) AF: 0.580 AC: 1220 AN: 2104

Alfa AF: 0.593 Hom.: 26380

Bravo AF: 0.542

Asia WGS AF: 0.635 AC: 2211 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.89
CADD	Benign	2.1
DANN	Benign	0.17
PhyloP100		0.49
Mutation Taster		=100/0	polymorphism (auto)

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

Other links and lift over

dbSNP: rs10801533; hg19: chr1-196395871;