7-150952457-CGAAGGGGATGGCGGCCACCATGTCGAT-C
Variant summary
Our verdict is Pathogenic. Variant got 15 ACMG points: 15P and 0B. PM1PM2PM4PP3PP5_Very_Strong
The ENST00000262186.10(KCNH2):c.1498_1524del(p.Ile500_Phe508del) variant causes a inframe deletion change involving the alteration of a conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. Variant has been reported in ClinVar as Pathogenic (★★). Synonymous variant affecting the same amino acid position (i.e. I500I) has been classified as Likely benign.
Frequency
Genomes: not found (cov: 33)
Consequence
KCNH2
ENST00000262186.10 inframe_deletion
ENST00000262186.10 inframe_deletion
Scores
Not classified
Clinical Significance
Conservation
PhyloP100: 9.80
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]
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ACMG classification
Classification made for transcript
Verdict is Pathogenic. Variant got 15 ACMG points.
PM1
In a hotspot region, there are 6 aminoacids with missense pathogenic changes in the window of +-8 aminoacids around while only 0 benign, 7 uncertain in ENST00000262186.10
PM2
Very rare variant in population databases, with high coverage;
PM4
Nonframeshift variant in NON repetitive region in ENST00000262186.10.
PP3
No computational evidence supports a deleterious effect, but strongly conserved according to phyloP
PP5
Variant 7-150952457-CGAAGGGGATGGCGGCCACCATGTCGAT-C is Pathogenic according to our data. Variant chr7-150952457-CGAAGGGGATGGCGGCCACCATGTCGAT-C is described in ClinVar as [Pathogenic]. Clinvar id is 200638.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr7-150952457-CGAAGGGGATGGCGGCCACCATGTCGAT-C is described in Lovd as [Pathogenic].
Transcripts
RefSeq
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | MANE | Protein | UniProt |
---|---|---|---|---|---|---|---|---|
KCNH2 | NM_000238.4 | c.1498_1524del | p.Ile500_Phe508del | inframe_deletion | 6/15 | ENST00000262186.10 | NP_000229.1 |
Ensembl
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | TSL | MANE | Protein | Appris | UniProt |
---|---|---|---|---|---|---|---|---|---|---|
KCNH2 | ENST00000262186.10 | c.1498_1524del | p.Ile500_Phe508del | inframe_deletion | 6/15 | 1 | NM_000238.4 | ENSP00000262186 | P1 |
Frequencies
GnomAD3 genomes Cov.: 33
GnomAD3 genomes
Cov.:
33
We have no GnomAD4 exomes data on this position. Probably position not covered by the project.
GnomAD4 genome Cov.: 33
GnomAD4 genome
Cov.:
33
ClinVar
Significance: Pathogenic
Submissions summary: Pathogenic:3
Revision: criteria provided, multiple submitters, no conflicts
LINK: link
Submissions by phenotype
Long QT syndrome 2 Pathogenic:1
Pathogenic, no assertion criteria provided | literature only | OMIM | Mar 10, 1995 | - - |
not provided Pathogenic:1
Pathogenic, criteria provided, single submitter | clinical testing | GeneDx | Apr 18, 2022 | Identified in a family with LQTS in the published literature (Curran et al., 1995); Not observed in large population cohorts (gnomAD); Published functional studies demonstrate a damaging effect as this variant yields a protein unable to form functional potassium channels and results in reduced capacity for potassium transport (Sanguinetti et al., 1996); In-frame deletion of 9 amino acids in a non-repeat region and disrupts the third membrane-spanning domain (S3) of KCNH2, causing loss of normal protein function; In silico analysis supports a deleterious effect on protein structure/function; This variant is associated with the following publications: (PMID: 10690299, 8700910, 7889573) - |
Long QT syndrome Pathogenic:1
Pathogenic, criteria provided, single submitter | clinical testing | Labcorp Genetics (formerly Invitae), Labcorp | Feb 28, 2023 | This variant, c.1498_1524del, results in the deletion of 9 amino acid(s) of the KCNH2 protein (p.Ile500_Phe508del), but otherwise preserves the integrity of the reading frame. This variant is not present in population databases (gnomAD no frequency). This variant has been observed in individual(s) with long QT syndrome (PMID: 7889573). It has also been observed to segregate with disease in related individuals. ClinVar contains an entry for this variant (Variation ID: 200638). For these reasons, this variant has been classified as Pathogenic. - |
Computational scores
Source:
Name
Calibrated prediction
Score
Prediction
Splicing
Find out detailed SpliceAI scores and Pangolin per-transcript scores at