U.S. flag

An official website of the United States government

NM_012210.4(TRIM32):c.469C>T (p.Arg157Trp) AND Bardet-Biedl syndrome

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Jan 8, 2024
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:
RCV002928620.2

Allele description

NM_012210.4(TRIM32):c.469C>T (p.Arg157Trp)

Genes:
ASTN2:astrotactin 2 [Gene - OMIM - HGNC]
TRIM32:tripartite motif containing 32 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
9q33.1
Genomic location:
Preferred name:
NM_012210.4(TRIM32):c.469C>T (p.Arg157Trp)
HGVS:
  • NC_000009.12:g.116698211C>T
  • NG_011619.1:g.15910C>T
  • NG_021409.2:g.721847G>A
  • NM_001099679.2:c.469C>T
  • NM_001365068.1:c.2806+27560G>AMANE SELECT
  • NM_001365069.1:c.2794+27560G>A
  • NM_001379048.1:c.469C>T
  • NM_001379049.1:c.469C>T
  • NM_001379050.1:c.469C>T
  • NM_012210.4:c.469C>TMANE SELECT
  • NM_014010.5:c.2653+27560G>A
  • NP_001093149.1:p.Arg157Trp
  • NP_001365977.1:p.Arg157Trp
  • NP_001365978.1:p.Arg157Trp
  • NP_001365979.1:p.Arg157Trp
  • NP_036342.2:p.Arg157Trp
  • NP_036342.2:p.Arg157Trp
  • LRG_211t1:c.469C>T
  • LRG_211:g.15910C>T
  • LRG_211p1:p.Arg157Trp
  • NC_000009.11:g.119460490C>T
  • NM_012210.3:c.469C>T
Protein change:
R157W
Molecular consequence:
  • NM_001365068.1:c.2806+27560G>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001365069.1:c.2794+27560G>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_014010.5:c.2653+27560G>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001099679.2:c.469C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001379048.1:c.469C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001379049.1:c.469C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001379050.1:c.469C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_012210.4:c.469C>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Bardet-Biedl syndrome (BBS)
Identifiers:
MONDO: MONDO:0015229; MedGen: C0752166; Orphanet: 110; OMIM: PS209900

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...

Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV003267246Invitae
criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))		Uncertain significance
(Jan 8, 2024) 		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

Sherloc: a comprehensive refinement of the ACMG-AMP variant classification criteria.

Nykamp K, Anderson M, Powers M, Garcia J, Herrera B, Ho YY, Kobayashi Y, Patil N, Thusberg J, Westbrook M; Invitae Clinical Genomics Group., Topper S.

Genet Med. 2017 Oct;19(10):1105-1117. doi: 10.1038/gim.2017.37. Epub 2017 May 11. Erratum in: Genet Med. 2020 Jan;22(1):240. doi: 10.1038/s41436-019-0624-9.

PubMed [citation]
PMID:
28492532
PMCID:
PMC5632818

Details of each submission

From Invitae, SCV003267246.2

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

Description

This sequence change replaces arginine, which is basic and polar, with tryptophan, which is neutral and slightly polar, at codon 157 of the TRIM32 protein (p.Arg157Trp). This variant is present in population databases (rs563191272, gnomAD 0.0009%). This variant has not been reported in the literature in individuals affected with TRIM32-related conditions. ClinVar contains an entry for this variant (Variation ID: 2058636). An algorithm developed to predict the effect of missense changes on protein structure and function (PolyPhen-2) suggests that this variant is likely to be disruptive. In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance.

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

Last Updated: Sep 1, 2024