NM_015999.6(ADIPOR1):c.703C>T (p.Arg235Trp) AND not provided

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Jun 11, 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:: RCV002597391.3

Allele description [Variation Report for NM_015999.6(ADIPOR1):c.703C>T (p.Arg235Trp)]

NM_015999.6(ADIPOR1):c.703C>T (p.Arg235Trp)

Gene:

ADIPOR1:adiponectin receptor 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

1q32.1

Genomic location:

Preferred name:

NM_015999.6(ADIPOR1):c.703C>T (p.Arg235Trp)

HGVS:

NC_000001.11:g.202943860G>A
NG_052860.1:g.19713C>T
NM_001127687.1:c.703C>T
NM_001290553.2:c.703C>T
NM_001290557.1:c.703C>T
NM_001290629.1:c.703C>T
NM_015999.6:c.703C>TMANE SELECT
NP_001121159.1:p.Arg235Trp
NP_001277482.1:p.Arg235Trp
NP_001277486.1:p.Arg235Trp
NP_001277558.1:p.Arg235Trp
NP_057083.2:p.Arg235Trp
NC_000001.10:g.202912988G>A

Protein change:

R235W

Molecular consequence:

NM_001127687.1:c.703C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001290553.2:c.703C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001290557.1:c.703C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001290629.1:c.703C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_015999.6:c.703C>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:: none provided
Identifiers:: MedGen: C3661900

Recent activity

Clear Turn Off Turn On

Tritrichomonas foetus strain K, whole genome shotgun sequencing project
Tritrichomonas foetus strain K, whole genome shotgun sequencing project
gi|1091437542|gb|MLAK00000000.1|MLA 0000

Nucleotide
Mus musculus bone marrow macrophage cDNA, RIKEN full-length enriched library, cl...
Mus musculus bone marrow macrophage cDNA, RIKEN full-length enriched library, clone:I830008N02 product:ADP-ribosylation factor-like 2 binding protein, full insert sequence
gi|74219720|dbj|AK150513.1|

Nucleotide
Mus musculus cDNA, clone:Y2G0116D15, strand:plus, reference:ENSEMBL:Mouse-Transc...
Mus musculus cDNA, clone:Y2G0116D15, strand:plus, reference:ENSEMBL:Mouse-Transcript-ENST:ENSMUST00000034228, based on BLAT search
gi|56033959|dbj|AK209782.1|

Nucleotide
Paraconiothyrium sp. strain KNUE 24S065 small subunit ribosomal RNA gene, partia...
Paraconiothyrium sp. strain KNUE 24S065 small subunit ribosomal RNA gene, partial sequence; internal transcribed spacer 1, 5.8S ribosomal RNA gene, and internal transcribed spacer 2, complete sequence; and large subunit ribosomal RNA gene, partial sequence
gi|2807268713|gb|PQ357223.1|

Nucleotide
Paraconiothyrium sp. isolate CCM-UEA-F0044 internal transcribed spacer 1, partia...
Paraconiothyrium sp. isolate CCM-UEA-F0044 internal transcribed spacer 1, partial sequence; 5.8S ribosomal RNA gene and internal transcribed spacer 2, complete sequence; and large subunit ribosomal RNA gene, partial sequence
gi|2716174933|gb|PP646503.1|

Nucleotide

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

Help

Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV002947783	Labcorp Genetics (formerly Invitae), Labcorp	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Uncertain significance (Jun 11, 2022)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV002947783

Labcorp Genetics (formerly Invitae), Labcorp

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Uncertain significance
(Jun 11, 2022)

germline

clinical testing

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

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	unknown	not provided	not provided	not provided	not provided	not provided	clinical 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, SCV002947783.2

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	PubMed (1)

Description

This sequence change replaces arginine, which is basic and polar, with tryptophan, which is neutral and slightly polar, at codon 235 of the ADIPOR1 protein (p.Arg235Trp). This variant is not present in population databases (gnomAD no frequency). This variant has not been reported in the literature in individuals affected with ADIPOR1-related conditions. Algorithms developed to predict the effect of missense changes on protein structure and function are either unavailable or do not agree on the potential impact of this missense change (SIFT: "Deleterious"; PolyPhen-2: "Benign"; Align-GVGD: "Class C0"). 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.

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Sep 29, 2024

ClinVar

Relating variation to medicine