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NM_032125.3(TMEM222):c.535G>A (p.Val179Ile) AND Inborn genetic diseases

Germline classification:
Likely benign (1 submission)
Last evaluated:
May 9, 2022
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:
RCV002946725.2

Allele description [Variation Report for NM_032125.3(TMEM222):c.535G>A (p.Val179Ile)]

NM_032125.3(TMEM222):c.535G>A (p.Val179Ile)

Gene:
TMEM222:transmembrane protein 222 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
1p36.11
Genomic location:
Preferred name:
NM_032125.3(TMEM222):c.535G>A (p.Val179Ile)
HGVS:
  • NC_000001.11:g.27334277G>A
  • NM_032125.3:c.535G>AMANE SELECT
  • NP_115501.2:p.Val179Ile
  • NC_000001.10:g.27660768G>A
  • NM_032125.2:c.535G>A
  • NR_037576.2:n.641G>A
  • NR_037577.2:n.488G>A
  • NR_037580.2:n.641G>A
Protein change:
V179I
Molecular consequence:
  • NM_032125.3:c.535G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NR_037576.2:n.641G>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NR_037577.2:n.488G>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NR_037580.2:n.641G>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

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

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Assertion and evidence details

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Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV003695075Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)		Likely benign
(May 9, 2022) 		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, SCV003695075.2

#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: May 1, 2024