rs869320733

chrX-101346635-GGCCCAGGCTT-G

Variant summary

Our verdict is Likely pathogenic. Variant got 8 ACMG points: 8P and 0B. PVS1_Strong PM2 PP5_Moderate

The NM_004085.4(TIMM8A):c.148_157del(p.Lys50GlnfsTer12) 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: 23)
• Consequence: TIMM8A NM_004085.4 frameshift
• Clinical Significance: Pathogenic criteria provided, single submitter P:2
• Conservation: PhyloP100: 9.70

Genes affected

TIMM8A (HGNC:11817): (translocase of inner mitochondrial membrane 8A) This translocase is involved in the import and insertion of hydrophobic membrane proteins from the cytoplasm into the mitochondrial inner membrane. The gene is mutated in Mohr-Tranebjaerg syndrome/Deafness Dystonia Syndrome (MTS/DDS) and it is postulated that MTS/DDS is a mitochondrial disease caused by a defective mitochondrial protein import system. Defects in this gene also cause Jensen syndrome; an X-linked disease with opticoacoustic nerve atrophy and muscle weakness. This protein, along with TIMM13, forms a 70 kDa heterohexamer. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, Mar 2009]

ACMG classification

Verdict is Likely_pathogenic. Variant got 8 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 4 pathogenic variants in the truncated region.
• PM2: Very rare variant in population databases, with high coverage
• PP5: Variant X-101346635-GGCCCAGGCTT-G is Pathogenic according to our data. Variant chrX-101346635-GGCCCAGGCTT-G is described in ClinVar as [Pathogenic]. Clinvar id is 11319.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-101346635-GGCCCAGGCTT-G is described in Lovd as [Pathogenic].

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
TIMM8A	NM_004085.4	c.148_157del	p.Lys50GlnfsTer12	frameshift_variant	2/2	ENST00000372902.4
TIMM8A	NM_001145951.2	c.*1742_*1751del		3_prime_UTR_variant	2/2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
TIMM8A	ENST00000372902.4	c.148_157del	p.Lys50GlnfsTer12	frameshift_variant	2/2	1	NM_004085.4	P1
TIMM8A	ENST00000644112.2	c.*1742_*1751del		3_prime_UTR_variant	2/2
TIMM8A	ENST00000647480.1	n.665_674del		non_coding_transcript_exon_variant	2/2
TIMM8A	ENST00000645279.1	c.*342_*351del		3_prime_UTR_variant, NMD_transcript_variant	3/3

Frequencies

GnomAD3 genomes Cov.: 23

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

GnomAD4 genome Cov.: 23

ClinVar

Significance: Pathogenic

Submissions summary: Pathogenic:2

Revision: criteria provided, single submitter

Submissions by phenotype

Deafness dystonia syndrome Pathogenic:2

Pathogenic, no assertion criteria provided	literature only	OMIM	Oct 01, 1996	- -
Pathogenic, criteria provided, single submitter	clinical testing	Baylor Genetics	May 01, 2023	- -

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: rs869320733; hg19: chrX-100601623;