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NM_001282448.2(TMEM262):c.59C>T (p.Thr20Met) AND not specified

Germline classification:
Likely benign (1 submission)
Last evaluated:
Nov 29, 2021
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:
RCV004211981.1

Allele description [Variation Report for NM_001282448.2(TMEM262):c.59C>T (p.Thr20Met)]

NM_001282448.2(TMEM262):c.59C>T (p.Thr20Met)

Gene:
TMEM262:transmembrane protein 262 [Gene - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
11q13.1
Genomic location:
Preferred name:
NM_001282448.2(TMEM262):c.59C>T (p.Thr20Met)
HGVS:
  • NC_000011.10:g.65088973G>A
  • NM_001242631.3:c.59C>T
  • NM_001282448.2:c.59C>TMANE SELECT
  • NP_001229560.1:p.Thr20Met
  • NP_001269377.1:p.Thr20Met
  • NC_000011.9:g.64856445G>A
  • NM_001242631.1:c.59C>T
Protein change:
T20M
Molecular consequence:
  • NM_001242631.3:c.59C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001282448.2:c.59C>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:
AllHighlyPenetrant
Identifiers:
MedGen: CN169374

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Assertion and evidence details

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Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV003706220Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)		Likely benign
(Nov 29, 2021) 		germlineclinical testing

Citation Link

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Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknownnot providednot providednot providednot providednot providedclinical testing

Details of each submission

From Ambry Genetics, SCV003706220.2

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided

Description

This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Nov 10, 2024