X-150657972-G-C

Variant names:

• chrX-150657972-G-C
• rs587783762
• NM_000252.3:c.1205G>C

Variant summary

Our verdict is Pathogenic. The variant received 12 ACMG points: 12P and 0B. PM1 PM2 PM5 PP3_Strong PP5_Moderate

The NM_000252.3(MTM1):​c.1205G>C​(p.Gly402Ala) variant causes a missense 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 (★). Another variant affecting the same amino acid position, but resulting in a different missense (i.e. G402V) has been classified as Pathogenic.

• Frequency: Genomes: not found (cov: 23)
• Consequence: MTM1 NM_000252.3 missense
• Clinical Significance: Pathogenic criteria provided, single submitter P:1
• Conservation: PhyloP100: 9.96
• Publications: 3 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.

• PM1: In a hotspot region, there are 6 aminoacids with missense pathogenic changes in the window of +-8 aminoacids around while only 2 benign, 3 uncertain in NM_000252.3
• PM2: Very rare variant in population databases, with high coverage
• PM5: Other missense variant is known to change same aminoacid residue: Variant chrX-150657972-G-T is described in CliVar as Pathogenic. Clinvar id is 1806312.Status of the report is criteria_provided_single_submitter, 1 stars.
• PP3: MetaRNN computational evidence supports a deleterious effect, 0.995
• PP5: Variant X-150657972-G-C is Pathogenic according to our data. Variant chrX-150657972-G-C is described in CliVar as Pathogenic. Clinvar id is 158904.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657972-G-C is described in CliVar as Pathogenic. Clinvar id is 158904.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657972-G-C is described in CliVar as Pathogenic. Clinvar id is 158904.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657972-G-C is described in CliVar as Pathogenic. Clinvar id is 158904.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657972-G-C is described in CliVar as Pathogenic. Clinvar id is 158904.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657972-G-C is described in CliVar as Pathogenic. Clinvar id is 158904.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657972-G-C is described in CliVar as Pathogenic. Clinvar id is 158904.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657972-G-C is described in CliVar as Pathogenic. Clinvar id is 158904.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657972-G-C is described in CliVar as Pathogenic. Clinvar id is 158904.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657972-G-C is described in CliVar as Pathogenic. Clinvar id is 158904.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657972-G-C is described in CliVar as Pathogenic. Clinvar id is 158904.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657972-G-C is described in CliVar as Pathogenic. Clinvar id is 158904.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657972-G-C is described in CliVar as Pathogenic. Clinvar id is 158904.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657972-G-C is described in CliVar as Pathogenic. Clinvar id is 158904.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657972-G-C is described in CliVar as Pathogenic. Clinvar id is 158904.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657972-G-C is described in CliVar as Pathogenic. Clinvar id is 158904.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657972-G-C is described in CliVar as Pathogenic. Clinvar id is 158904.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657972-G-C is described in CliVar as Pathogenic. Clinvar id is 158904.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657972-G-C is described in CliVar as Pathogenic. Clinvar id is 158904.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657972-G-C is described in CliVar as Pathogenic. Clinvar id is 158904.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657972-G-C is described in CliVar as Pathogenic. Clinvar id is 158904.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657972-G-C is described in CliVar as Pathogenic. Clinvar id is 158904.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657972-G-C is described in CliVar as Pathogenic. Clinvar id is 158904.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657972-G-C is described in CliVar as Pathogenic. Clinvar id is 158904.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657972-G-C is described in CliVar as Pathogenic. Clinvar id is 158904.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657972-G-C is described in CliVar as Pathogenic. Clinvar id is 158904.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657972-G-C is described in CliVar as Pathogenic. Clinvar id is 158904.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657972-G-C is described in CliVar as Pathogenic. Clinvar id is 158904.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657972-G-C is described in CliVar as Pathogenic. Clinvar id is 158904.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657972-G-C is described in CliVar as Pathogenic. Clinvar id is 158904.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657972-G-C is described in CliVar as Pathogenic. Clinvar id is 158904.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657972-G-C is described in CliVar as Pathogenic. Clinvar id is 158904.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657972-G-C is described in CliVar as Pathogenic. Clinvar id is 158904.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657972-G-C is described in CliVar as Pathogenic. Clinvar id is 158904.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657972-G-C is described in CliVar as Pathogenic. Clinvar id is 158904.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657972-G-C is described in CliVar as Pathogenic. Clinvar id is 158904.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657972-G-C is described in CliVar as Pathogenic. Clinvar id is 158904.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657972-G-C is described in CliVar as Pathogenic. Clinvar id is 158904.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657972-G-C is described in CliVar as Pathogenic. Clinvar id is 158904.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657972-G-C is described in CliVar as Pathogenic. Clinvar id is 158904.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657972-G-C is described in CliVar as Pathogenic. Clinvar id is 158904.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657972-G-C is described in CliVar as Pathogenic. Clinvar id is 158904.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657972-G-C is described in CliVar as Pathogenic. Clinvar id is 158904.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657972-G-C is described in CliVar as Pathogenic. Clinvar id is 158904.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657972-G-C is described in CliVar as Pathogenic. Clinvar id is 158904.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657972-G-C is described in CliVar as Pathogenic. Clinvar id is 158904.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657972-G-C is described in CliVar as Pathogenic. Clinvar id is 158904.Status of the report is criteria_provided_single_submitter, 1 stars. Variant chrX-150657972-G-C is described in CliVar as Pathogenic. Clinvar id is 158904.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.1205G>C	p.Gly402Ala	missense_variant	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.1205G>C	p.Gly402Ala	missense_variant	Exon 11 of 15	1	NM_000252.3	ENSP00000359423.3

Frequencies

GnomAD3 genomes Cov.: 23

GnomAD4 exome Cov.: 30

GnomAD4 genome Cov.: 23

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

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Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Pathogenic	0.95
BayesDel_addAF	Pathogenic	0.73	D
BayesDel_noAF	Pathogenic	0.82
CADD	Pathogenic	28
DANN	Uncertain	1.0
DEOGEN2	Pathogenic	0.99	D
FATHMM_MKL	Pathogenic	1.0	D
LIST_S2	Pathogenic	0.99	D
M_CAP	Pathogenic	0.75	D
MetaRNN	Pathogenic	0.99	D
MetaSVM	Pathogenic	1.0	D
MutationAssessor	Pathogenic	4.2	H
PhyloP100		10
PrimateAI	Uncertain	0.65	T
PROVEAN	Pathogenic	-5.8	D
REVEL	Pathogenic	0.94
Sift	Pathogenic	0.0	D
Sift4G	Uncertain	0.025	D
Polyphen		1.0	D
Vest4		0.98
MutPred		0.99		Gain of helix (P = 0.2294);
MVP		1.0
MPC		1.5
ClinPred		1.0	D
GERP RS		4.5
Varity_R		0.98
gMVP		0.98
Mutation Taster		=1/99	disease causing (ClinVar)

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.090		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: rs587783762; hg19: chrX-149826445;