5-173233064-CTG-AACGGTAC

Position:

• chr5-173233064-CTG-AACGGTAC

Variant summary

Our verdict is Pathogenic. Variant got 18 ACMG points: 18P and 0B. PVS1 PM2 PP5_Very_Strong

The NM_004387.4(NKX2-5):​c.478_480delinsGTACCGTT​(p.Gln160ValfsTer18) variant causes a frameshift 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 (★★).

• Frequency: Genomes: not found (cov: 32)
• Consequence: NKX2-5 NM_004387.4 frameshift
• Clinical Significance: Pathogenic criteria provided, multiple submitters, no conflicts P:2
• Conservation: PhyloP100: 9.97

Genes affected

NKX2-5 (HGNC:2488): (NK2 homeobox 5) This gene encodes a homeobox-containing transcription factor. This transcription factor functions in heart formation and development. Mutations in this gene cause atrial septal defect with atrioventricular conduction defect, and also tetralogy of Fallot, which are both heart malformation diseases. Mutations in this gene can also cause congenital hypothyroidism non-goitrous type 5, a non-autoimmune condition. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]

ACMG classification

Verdict is Pathogenic. Variant got 18 ACMG points.

• PVS1: Loss of function variant, product does not undergo nonsense mediated mRNA decay. Variant is located in the 3'-most exon, not predicted to undergo nonsense mediated mRNA decay. There are 122 pathogenic variants in the truncated region.
• PM2: Very rare variant in population databases, with high coverage
• PP5: Variant 5-173233064-CTG-AACGGTAC is Pathogenic according to our data. Variant chr5-173233064-CTG-AACGGTAC is described in ClinVar as [Pathogenic]. Clinvar id is 211670.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
NKX2-5	NM_004387.4	c.478_480delinsGTACCGTT	p.Gln160ValfsTer18	frameshift_variant	2/2	ENST00000329198.5
NKX2-5	NM_001166175.2	c.*431_*433delinsGTACCGTT		3_prime_UTR_variant	2/2
NKX2-5	NM_001166176.2	c.*277_*279delinsGTACCGTT		3_prime_UTR_variant	2/2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
NKX2-5	ENST00000329198.5	c.478_480delinsGTACCGTT	p.Gln160ValfsTer18	frameshift_variant	2/2	1	NM_004387.4	P1
NKX2-5	ENST00000424406.2	c.*431_*433delinsGTACCGTT		3_prime_UTR_variant	2/2	1
NKX2-5	ENST00000521848.1	c.*277_*279delinsGTACCGTT		3_prime_UTR_variant	2/2	2

Frequencies

GnomAD3 genomes Cov.: 32

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

GnomAD4 genome Cov.: 32

ClinVar

Significance: Pathogenic

Submissions summary: Pathogenic:2

Revision: criteria provided, multiple submitters, no conflicts

Submissions by phenotype

Abnormal cardiovascular system morphology Pathogenic:1

Pathogenic, criteria provided, single submitter

clinical testing

Genetic Services Laboratory, University of Chicago

Feb 08, 2013

- -

not provided Pathogenic:1

Pathogenic, criteria provided, single submitter

clinical testing

GeneDx

Jan 06, 2017

Although the c.478_480delCAGinsGTACCGTT pathogenic variant in the NKX2-5 gene has not been reported to our knowledge, this variant causes a shift in reading frame starting at codon Glutamine 160, changing it to a Valine, and creating a premature stop codon at position 18 of the new reading frame, denoted p.Gln160ValfsX18. This pathogenic variant is expected to result in an abnormal, truncated protein product. Other frameshift variants in the NKX2-5 gene have been reported in HGMD in association with NKX2-5-related disorders (Stenson et al., 2014). Furthermore, the c.478_480delCAGinsGTACCGTT variant was not observed in approximately 6,500 individuals of European and African American ancestry in the NHLBI Exome Sequencing Project, indicating it is not a common benign variant in these populations. -

Computational scores

Source: dbNSFP v4.3

Splicing

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

Publications

LitVar

Other links and lift over

dbSNP: rs797045790; hg19: chr5-172660067;