NM_004535.3(MYT1):c.976C>T (p.Pro326Ser) AND Inborn genetic diseases

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Nov 14, 2023
Review status:: 1 star out of maximum of 4 stars
criteria provided, single submitter

Somatic classification of clinical impact:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Somatic classification of oncogenicity:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Record status:: current
Accession:: RCV004460511.1

Allele description [Variation Report for NM_004535.3(MYT1):c.976C>T (p.Pro326Ser)]

NM_004535.3(MYT1):c.976C>T (p.Pro326Ser)

Gene:

MYT1:myelin transcription factor 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

20q13.33

Genomic location:

Preferred name:

NM_004535.3(MYT1):c.976C>T (p.Pro326Ser)

HGVS:

NC_000020.11:g.64208172C>T
NM_004535.3:c.976C>TMANE SELECT
NP_004526.1:p.Pro326Ser
NC_000020.10:g.62839525C>T
NM_004535.2:c.976C>T

Protein change:

P326S

Molecular consequence:

NM_004535.3:c.976C>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Inborn genetic diseases
Identifiers:: MeSH: D030342; MedGen: C0950123

Recent activity

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Microbe sample from Streptococcus suis
Microbe sample from Streptococcus suis

biosample
restriction endonuclease subunit S, partial [Mycoplasmoides pneumoniae]
restriction endonuclease subunit S, partial [Mycoplasmoides pneumoniae]
gi|2572915427|ref|WP_308189452.1|

Protein
thymidylate synthase [Mycoplasmoides pneumoniae]
thymidylate synthase [Mycoplasmoides pneumoniae]
gi|740749201|ref|WP_038534485.1|

Protein
restriction endonuclease subunit S [Mycoplasmoides pneumoniae]
restriction endonuclease subunit S [Mycoplasmoides pneumoniae]
gi|740749105|ref|WP_038534389.1|

Protein
Streptococcus suis strain 2017UMN1435.22, whole genome shotgun sequencing projec...
Streptococcus suis strain 2017UMN1435.22, whole genome shotgun sequencing project
gi|1697740115|gb|VIEI00000000.1|VIE 0000

Nucleotide

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV004957213	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (Nov 14, 2023)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV004957213

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(Nov 14, 2023)

germline

clinical testing

Citation Link

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From Ambry Genetics, SCV004957213.1

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	not provided

Description

The c.976C>T (p.P326S) alteration is located in exon 7 (coding exon 5) of the MYT1 gene. This alteration results from a C to T substitution at nucleotide position 976, causing the proline (P) at amino acid position 326 to be replaced by a serine (S). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: May 7, 2024

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