2-199925635-CATTCTGGAGGAAGCAAT-C

Position:

• chr2-199925635-CATTCTGGAGGAAGCAAT-C

Variant summary

Our verdict is Likely pathogenic. Variant got 7 ACMG points: 7P and 0B. PVS1_Strong PM2 PP5

The NM_153689.6(C2orf69):​c.909_925del​(p.Ser304LeufsTer29) 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 (no stars).

• Frequency: Genomes: not found (cov: 32)
• Consequence: C2orf69 NM_153689.6 frameshift
• Clinical Significance: Pathogenic no assertion criteria provided P:1
• Conservation: PhyloP100: 10.0

Genes affected

C2orf69 (HGNC:26799): (chromosome 2 open reading frame 69) Involved in oxidative phosphorylation. Located in mitochondrion. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

Verdict is Likely_pathogenic. Variant got 7 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. Fraction of 0.216 CDS is truncated, and there are 1 pathogenic variants in the truncated region.
• PM2: Very rare variant in population databases, with high coverage
• PP5: Variant 2-199925635-CATTCTGGAGGAAGCAAT-C is Pathogenic according to our data. Variant chr2-199925635-CATTCTGGAGGAAGCAAT-C is described in ClinVar as [Pathogenic]. Clinvar id is 1177458.Status of the report is no_assertion_criteria_provided, 0 stars. Variant chr2-199925635-CATTCTGGAGGAAGCAAT-C is described in Lovd as [Pathogenic].

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
C2orf69	NM_153689.6	c.909_925del	p.Ser304LeufsTer29	frameshift_variant	2/2	ENST00000319974.6	NP_710156.3

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
C2orf69	ENST00000319974.6	c.909_925del	p.Ser304LeufsTer29	frameshift_variant	2/2	1	NM_153689.6	ENSP00000312770	P1
C2orf69	ENST00000491721.1	n.466+13866_466+13882del		intron_variant, non_coding_transcript_variant		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:1

Revision: no assertion criteria provided

Submissions by phenotype

Combined oxidative phosphorylation deficiency 53 Pathogenic:1

Pathogenic, no assertion criteria provided

literature only

OMIM

Jul 09, 2021

- -

Computational scores

Source: dbNSFP v4.3

Splicing

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

Publications

No publications associated with this variant yet.

Other links and lift over

hg19: chr2-200790358;