U.S. flag

An official website of the United States government

NM_174878.3(CLRN1):c.406G>A (p.Gly136Arg) AND not provided

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Oct 17, 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:
RCV002542940.2

Allele description [Variation Report for NM_174878.3(CLRN1):c.406G>A (p.Gly136Arg)]

NM_174878.3(CLRN1):c.406G>A (p.Gly136Arg)

Gene:
CLRN1:clarin 1 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
3q25.1
Genomic location:
Preferred name:
NM_174878.3(CLRN1):c.406G>A (p.Gly136Arg)
HGVS:
  • NC_000003.12:g.150941609C>T
  • NG_009168.1:g.36391G>A
  • NM_001195794.1:c.406G>A
  • NM_001256819.2:c.*20G>A
  • NM_052995.2:c.178G>A
  • NM_174878.3:c.406G>AMANE SELECT
  • NP_001182723.1:p.Gly136Arg
  • NP_443721.1:p.Gly60Arg
  • NP_777367.1:p.Gly136Arg
  • LRG_700t1:c.406G>A
  • LRG_700t2:c.178G>A
  • LRG_700:g.36391G>A
  • LRG_700p1:p.Gly136Arg
  • LRG_700p2:p.Gly60Arg
  • NC_000003.11:g.150659396C>T
  • NR_046380.3:n.576G>A
Protein change:
G136R
Links:
dbSNP: rs904836940
NCBI 1000 Genomes Browser:
rs904836940
Molecular consequence:
  • NM_001256819.2:c.*20G>A - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
  • NM_001195794.1:c.406G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_052995.2:c.178G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_174878.3:c.406G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NR_046380.3:n.576G>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Synonyms:
none provided
Identifiers:
MedGen: C3661900

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
SCV003487004Labcorp Genetics (formerly Invitae), Labcorp
criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))		Uncertain significance
(Oct 17, 2022) 		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 Labcorp Genetics (formerly Invitae), Labcorp, SCV003487004.1

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

Description

This sequence change replaces glycine, which is neutral and non-polar, with arginine, which is basic and polar, at codon 136 of the CLRN1 protein (p.Gly136Arg). This variant is present in population databases (no rsID available, gnomAD 0.002%). This variant has not been reported in the literature in individuals affected with CLRN1-related conditions. ClinVar contains an entry for this variant (Variation ID: 991769). Algorithms developed to predict the effect of missense changes on protein structure and function (SIFT, PolyPhen-2, Align-GVGD) all suggest 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 29, 2024