7-150951704-C-T

Variant names:

• chr7-150951704-C-T
• rs199473517
• NM_000238.4:c.1689G>A

Variant summary

Our verdict is Pathogenic. The variant received 18 ACMG points: 18P and 0B. PVS1 PM2 PP5_Very_Strong

The NM_000238.4(KCNH2):​c.1689G>A​(p.Trp563*) variant causes a stop gained change. The variant was absent in control chromosomes in GnomAD project. In-silico tool predicts a pathogenic outcome for this variant. Variant has been reported in ClinVar as Pathogenic (★★). Variant results in nonsense mediated mRNA decay.

• Frequency: Genomes: not found (cov: 34)
• Consequence: KCNH2 NM_000238.4 stop_gained
• Clinical Significance: Pathogenic criteria provided, multiple submitters, no conflicts P:2
• Conservation: PhyloP100: 5.89
• Publications: 5 publications found

Genes affected

KCNH2 (HGNC:6251): (potassium voltage-gated channel subfamily H member 2) This gene encodes a component of a voltage-activated potassium channel found in cardiac muscle, nerve cells, and microglia. Four copies of this protein interact with one copy of the KCNE2 protein to form a functional potassium channel. Mutations in this gene can cause long QT syndrome type 2 (LQT2). Transcript variants encoding distinct isoforms have been identified. [provided by RefSeq, May 2022]

KCNH2 Gene-Disease associations (from GenCC):

• long QT syndrome

  Inheritance: AD Classification: DEFINITIVE Submitted by: ClinGen
• long QT syndrome 2

  Inheritance: AD Classification: DEFINITIVE, STRONG Submitted by: Labcorp Genetics (formerly Invitae), Ambry Genetics, G2P
• short QT syndrome

  Inheritance: AD Classification: DEFINITIVE, SUPPORTIVE Submitted by: Orphanet, ClinGen
• short QT syndrome type 1

  Inheritance: AD Classification: DEFINITIVE, STRONG, MODERATE Submitted by: Labcorp Genetics (formerly Invitae), G2P, Ambry Genetics
• Brugada syndrome

  Inheritance: AD Classification: MODERATE, NO_KNOWN Submitted by: ClinGen, Genomics England PanelApp

ACMG classification

Our verdict: Pathogenic. The variant received 18 ACMG points.

• PVS1: Loss of function variant, product undergoes nonsense mediated mRNA decay. LoF is a known mechanism of disease.
• PM2: Very rare variant in population databases, with high coverage
• PP5: Variant 7-150951704-C-T is Pathogenic according to our data. Variant chr7-150951704-C-T is described in CliVar as Pathogenic. Clinvar id is 526968.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-150951704-C-T is described in CliVar as Pathogenic. Clinvar id is 526968.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-150951704-C-T is described in CliVar as Pathogenic. Clinvar id is 526968.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-150951704-C-T is described in CliVar as Pathogenic. Clinvar id is 526968.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-150951704-C-T is described in CliVar as Pathogenic. Clinvar id is 526968.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-150951704-C-T is described in CliVar as Pathogenic. Clinvar id is 526968.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-150951704-C-T is described in CliVar as Pathogenic. Clinvar id is 526968.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-150951704-C-T is described in CliVar as Pathogenic. Clinvar id is 526968.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-150951704-C-T is described in CliVar as Pathogenic. Clinvar id is 526968.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-150951704-C-T is described in CliVar as Pathogenic. Clinvar id is 526968.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-150951704-C-T is described in CliVar as Pathogenic. Clinvar id is 526968.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-150951704-C-T is described in CliVar as Pathogenic. Clinvar id is 526968.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-150951704-C-T is described in CliVar as Pathogenic. Clinvar id is 526968.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-150951704-C-T is described in CliVar as Pathogenic. Clinvar id is 526968.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
KCNH2	NM_000238.4	c.1689G>A	p.Trp563*	stop_gained	Exon 7 of 15	ENST00000262186.10	NP_000229.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
KCNH2	ENST00000262186.10	c.1689G>A	p.Trp563*	stop_gained	Exon 7 of 15	1	NM_000238.4	ENSP00000262186.5

Frequencies

GnomAD3 genomes Cov.: 34

GnomAD4 exome Cov.: 36

GnomAD4 genome Cov.: 34

ClinVar

Significance: Pathogenic

Submissions summary: Pathogenic:2

Revision: criteria provided, multiple submitters, no conflicts

Submissions by phenotype

not provided Pathogenic:1

Jun 06, 2018

GeneDx

Significance: Pathogenic

Review Status: criteria provided, single submitter

Collection Method: clinical testing

The W563X variant in the KCNH2 gene has been reported in one family with LQTS (Itoh et al., 2016). The W563X variant is predicted to cause loss of normal protein function either by protein truncation or nonsense-mediated mRNA decay. Other nonsense variants in the KCNH2 gene have been reported in Human Gene Mutation Database in association with LQTS (Stenson et al., 2014). Furthermore, the W563X variant is not observed in large population cohorts (Lek et al., 2016). In summary, W563X in the KCNH2 gene is interpreted as a pathogenic variant. -

Long QT syndrome Pathogenic:1

Oct 05, 2017

Labcorp Genetics (formerly Invitae), Labcorp

Significance: Pathogenic

Review Status: criteria provided, single submitter

Collection Method: clinical testing

This variant is not present in population databases (ExAC no frequency). This variant has not been reported in the literature in individuals with KCNH2-related disease. Loss-of-function variants in KCNH2 are known to be pathogenic (PMID: 19862833). For these reasons, this variant has been classified as Pathogenic. This sequence change creates a premature translational stop signal (p.Trp563*) in the KCNH2 gene. It is expected to result in an absent or disrupted protein product. -

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_addAF	Pathogenic	0.56	D
BayesDel_noAF	Pathogenic	0.57
CADD	Pathogenic	42
DANN	Uncertain	1.0
Eigen	Pathogenic	0.70
Eigen_PC	Uncertain	0.53
FATHMM_MKL	Uncertain	0.96	D
PhyloP100		5.9
Vest4		0.84
GERP RS		3.5
RBP_binding_hub_radar		0.0
RBP_regulation_power_radar		1.7
Mutation Taster		=0/200	disease causing (ClinVar)

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.030		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: rs199473517; hg19: chr7-150648792;