rs552322812

Variant names:

• chr10-76884892-CTTTTTT-C
• rs552322812
• NM_001161352.2:c.*2368_*2373delAAAAAA

Your query was ambiguous. Multiple possible variants found:

• chr10-76884892-CTTTTTT-C
• chr10-76884892-CTTTTTT-CTTT
• chr10-76884892-CTTTTTT-CTTTT
• chr10-76884892-CTTTTTT-CTTTTT
• chr10-76884892-CTTTTTT-CTTTTTTT
• chr10-76884892-CTTTTTT-CTTTTTTTT

Variant summary

Our verdict is Uncertain significance. The variant received 2 ACMG points: 2P and 0B. PM2

The NM_001161352.2(KCNMA1):​c.*2368_*2373delAAAAAA variant causes a 3 prime UTR change. The variant allele was found at a frequency of 0.00000243 in 1,234,552 control chromosomes in the GnomAD database, with no homozygous occurrence. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency:
  • Genomes: not found (cov: 30)
  • Exomes 𝑓: 0.0000024 (0 hom.)
• Consequence: KCNMA1 NM_001161352.2 3_prime_UTR
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 4.24
• Publications: 0 publications found

Genes affected

KCNMA1 (HGNC:6284): (potassium calcium-activated channel subfamily M alpha 1) This gene encodes the alpha subunit of calcium-activated BK channel. The encoded protein is involved in several physiological processes including smooth muscle contraction, neurotransmitter release and neuronal excitability. Mutations in this gene are associated with a spectrum of neurological disorders including Paroxysmal Nonkinesigenic Dyskinesia 3, Idiopathic Generalized Epilepsy 16 and Liang-Wang syndrome. [provided by RefSeq, Aug 2022]

KCNMA1 Gene-Disease associations (from GenCC):

• generalized epilepsy-paroxysmal dyskinesia syndrome

  Inheritance: AD, AR Classification: DEFINITIVE, STRONG, MODERATE, SUPPORTIVE Submitted by: Illumina, G2P, Ambry Genetics, Orphanet, Labcorp Genetics (formerly Invitae), ClinGen
• Liang-Wang syndrome

  Inheritance: AD Classification: STRONG Submitted by: Ambry Genetics
• cerebellar atrophy, developmental delay, and seizures

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

ACMG classification

Our verdict: Uncertain_significance. The variant received 2 ACMG points.

• PM2: Very rare variant in population databases, with high coverage

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
KCNMA1	NM_001161352.2	c.*2368_*2373delAAAAAA		3_prime_UTR_variant	Exon 28 of 28	ENST00000286628.14	NP_001154824.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
KCNMA1	ENST00000286628.14	c.*2368_*2373delAAAAAA		3_prime_UTR_variant	Exon 28 of 28	1	NM_001161352.2	ENSP00000286628.8

Frequencies

GnomAD3 genomes Cov.: 30

GnomAD4 exome AF: 0.00000243 AC: 3 AN: 1234552 Hom.: 0 AF XY: 0.00000165 AC XY: 1 AN XY: 604312

African (AFR) AF: 0.00 AC: 0 AN: 25472

American (AMR) AF: 0.00 AC: 0 AN: 17146

Ashkenazi Jewish (ASJ) AF: 0.00 AC: 0 AN: 19920

East Asian (EAS) AF: 0.00 AC: 0 AN: 29972

South Asian (SAS) AF: 0.00 AC: 0 AN: 54340

European-Finnish (FIN) AF: 0.0000703 AC: 3 AN: 42684

Middle Eastern (MID) AF: 0.00 AC: 0 AN: 5100

European-Non Finnish (NFE) AF: 0.00 AC: 0 AN: 989520

Other (OTH) AF: 0.00 AC: 0 AN: 50398

GnomAD4 genome Cov.: 30

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
PhyloP100		4.2

Splicing

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

Other links and lift over

dbSNP: rs552322812; hg19: chr10-78644650;