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NM_001252024.2(TRPM1):c.2633G>A (p.Trp878Ter) AND TRPM1-related disorder

Germline classification:
Pathogenic (1 submission)
Last evaluated:
Jan 17, 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:
RCV003413796.4

Allele description [Variation Report for NM_001252024.2(TRPM1):c.2633G>A (p.Trp878Ter)]

NM_001252024.2(TRPM1):c.2633G>A (p.Trp878Ter)

Gene:
TRPM1:transient receptor potential cation channel subfamily M member 1 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
15q13.3
Genomic location:
Preferred name:
NM_001252024.2(TRPM1):c.2633G>A (p.Trp878Ter)
HGVS:
  • NC_000015.10:g.31035613C>T
  • NG_016453.2:g.130661G>A
  • NM_001252020.2:c.2684G>A
  • NM_001252024.2:c.2633G>AMANE SELECT
  • NM_002420.6:c.2567G>A
  • NP_001238949.1:p.Trp895Ter
  • NP_001238953.1:p.Trp878Ter
  • NP_002411.3:p.Trp856Ter
  • NC_000015.9:g.31327816C>T
  • NM_002420.5:c.2567G>A
Protein change:
W856*
Links:
dbSNP: rs765645888
NCBI 1000 Genomes Browser:
rs765645888
Molecular consequence:
  • NM_001252020.2:c.2684G>A - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001252024.2:c.2633G>A - nonsense - [Sequence Ontology: SO:0001587]
  • NM_002420.6:c.2567G>A - nonsense - [Sequence Ontology: SO:0001587]

Condition(s)

Name:
TRPM1-related disorder
Synonyms:
TRPM1-related condition
Identifiers:

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV004118478PreventionGenetics, part of Exact Sciences
criteria provided, single submitter

(ACMG Guidelines, 2015)		Pathogenic
(Jan 17, 2023) 		germlineclinical testing

PubMed (1)
[See all records that cite this PMID]

Help

Summary from all submissions

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

Citations

PubMed

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee..

Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.

PubMed [citation]
PMID:
25741868
PMCID:
PMC4544753

Details of each submission

From PreventionGenetics, part of Exact Sciences, SCV004118478.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)

Description

The TRPM1 c.2567G>A variant is predicted to result in premature protein termination (p.Trp856*). This variant has been reported apparently homozygous in one patient with complete congenital stationary night blindness, myopia, nystagmus and strabismus (Patient 691, Table 1, Audo et al. 2009. PubMed ID: 19896113). This variant is reported in 0.00088% of alleles in individuals of European (Non-Finnish) descent in gnomAD (http://gnomad.broadinstitute.org/variant/15-31327816-C-T). Nonsense variants in TRPM1 are expected to be pathogenic. This variant is interpreted as pathogenic.

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

Last Updated: May 26, 2024