NM_000252.3:c.1232G>A

Variant names:

• chrX-150657999-G-A
• rs587783763
• NM_000252.3:c.1232G>A

Variant summary

Our verdict is Pathogenic. The variant received 12 ACMG points: 12P and 0B. PVS1 PM2 PP5_Moderate

The NM_000252.3(MTM1):​c.1232G>A​(p.Trp411*) variant causes a stop gained change involving the alteration of a conserved nucleotide. 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: 23)
• Consequence: MTM1 NM_000252.3 stop_gained
• Clinical Significance: Pathogenic criteria provided, single submitter P:1
• Conservation: PhyloP100: 9.96
• Publications: 2 publications found

Genes affected

MTM1 (HGNC:7448): (myotubularin 1) This gene encodes a dual-specificity phosphatase that acts on both phosphotyrosine and phosphoserine. It is required for muscle cell differentiation and mutations in this gene have been identified as being responsible for X-linked myotubular myopathy. [provided by RefSeq, Jul 2008]

MTM1 Gene-Disease associations (from GenCC):

• X-linked myotubular myopathy

  Inheritance: XL Classification: DEFINITIVE, STRONG, MODERATE, SUPPORTIVE Submitted by: G2P, Ambry Genetics, Genomics England PanelApp, Labcorp Genetics (formerly Invitae), ClinGen, Myriad Women’s Health, Orphanet

ACMG classification

Our verdict: Pathogenic. The variant received 12 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 X-150657999-G-A is Pathogenic according to our data. Variant chrX-150657999-G-A is described in CliVar as Pathogenic. Clinvar id is 158905.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657999-G-A is described in CliVar as Pathogenic. Clinvar id is 158905.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657999-G-A is described in CliVar as Pathogenic. Clinvar id is 158905.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657999-G-A is described in CliVar as Pathogenic. Clinvar id is 158905.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657999-G-A is described in CliVar as Pathogenic. Clinvar id is 158905.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657999-G-A is described in CliVar as Pathogenic. Clinvar id is 158905.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657999-G-A is described in CliVar as Pathogenic. Clinvar id is 158905.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657999-G-A is described in CliVar as Pathogenic. Clinvar id is 158905.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657999-G-A is described in CliVar as Pathogenic. Clinvar id is 158905.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657999-G-A is described in CliVar as Pathogenic. Clinvar id is 158905.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657999-G-A is described in CliVar as Pathogenic. Clinvar id is 158905.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657999-G-A is described in CliVar as Pathogenic. Clinvar id is 158905.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657999-G-A is described in CliVar as Pathogenic. Clinvar id is 158905.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657999-G-A is described in CliVar as Pathogenic. Clinvar id is 158905.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657999-G-A is described in CliVar as Pathogenic. Clinvar id is 158905.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657999-G-A is described in CliVar as Pathogenic. Clinvar id is 158905.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657999-G-A is described in CliVar as Pathogenic. Clinvar id is 158905.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657999-G-A is described in CliVar as Pathogenic. Clinvar id is 158905.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657999-G-A is described in CliVar as Pathogenic. Clinvar id is 158905.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657999-G-A is described in CliVar as Pathogenic. Clinvar id is 158905.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657999-G-A is described in CliVar as Pathogenic. Clinvar id is 158905.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657999-G-A is described in CliVar as Pathogenic. Clinvar id is 158905.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657999-G-A is described in CliVar as Pathogenic. Clinvar id is 158905.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657999-G-A is described in CliVar as Pathogenic. Clinvar id is 158905.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657999-G-A is described in CliVar as Pathogenic. Clinvar id is 158905.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657999-G-A is described in CliVar as Pathogenic. Clinvar id is 158905.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657999-G-A is described in CliVar as Pathogenic. Clinvar id is 158905.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657999-G-A is described in CliVar as Pathogenic. Clinvar id is 158905.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657999-G-A is described in CliVar as Pathogenic. Clinvar id is 158905.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657999-G-A is described in CliVar as Pathogenic. Clinvar id is 158905.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657999-G-A is described in CliVar as Pathogenic. Clinvar id is 158905.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657999-G-A is described in CliVar as Pathogenic. Clinvar id is 158905.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657999-G-A is described in CliVar as Pathogenic. Clinvar id is 158905.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657999-G-A is described in CliVar as Pathogenic. Clinvar id is 158905.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657999-G-A is described in CliVar as Pathogenic. Clinvar id is 158905.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657999-G-A is described in CliVar as Pathogenic. Clinvar id is 158905.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657999-G-A is described in CliVar as Pathogenic. Clinvar id is 158905.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657999-G-A is described in CliVar as Pathogenic. Clinvar id is 158905.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657999-G-A is described in CliVar as Pathogenic. Clinvar id is 158905.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657999-G-A is described in CliVar as Pathogenic. Clinvar id is 158905.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657999-G-A is described in CliVar as Pathogenic. Clinvar id is 158905.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657999-G-A is described in CliVar as Pathogenic. Clinvar id is 158905.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657999-G-A is described in CliVar as Pathogenic. Clinvar id is 158905.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657999-G-A is described in CliVar as Pathogenic. Clinvar id is 158905.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657999-G-A is described in CliVar as Pathogenic. Clinvar id is 158905.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657999-G-A is described in CliVar as Pathogenic. Clinvar id is 158905.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657999-G-A is described in CliVar as Pathogenic. Clinvar id is 158905.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657999-G-A is described in CliVar as Pathogenic. Clinvar id is 158905.Status of the report is criteria_provided_single_submitter, 1 stars.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
MTM1	NM_000252.3	c.1232G>A	p.Trp411*	stop_gained	Exon 11 of 15	ENST00000370396.7	NP_000243.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
MTM1	ENST00000370396.7	c.1232G>A	p.Trp411*	stop_gained	Exon 11 of 15	1	NM_000252.3	ENSP00000359423.3

Frequencies

GnomAD3 genomes Cov.: 23

GnomAD4 exome Cov.: 30

GnomAD4 genome Cov.: 23

Alfa AF: 0.00 Hom.: 0

ClinVar

Significance: Pathogenic

Submissions summary: Pathogenic:1

Revision: criteria provided, single submitter

Submissions by phenotype

Severe X-linked myotubular myopathy Pathogenic:1

Feb 08, 2013

Genetic Services Laboratory, University of Chicago

Significance: Pathogenic

Review Status: criteria provided, single submitter

Collection Method: clinical testing

- -

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_addAF	Pathogenic	0.74	D
BayesDel_noAF	Pathogenic	0.66
CADD	Pathogenic	48
DANN	Uncertain	1.0
FATHMM_MKL	Pathogenic	1.0	D
PhyloP100		10
Vest4		0.99
GERP RS		5.5
Mutation Taster		=0/200	disease causing (ClinVar)

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.18		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: rs587783763; hg19: chrX-149826472; COSMIC: COSV60334819;