U.S. flag

An official website of the United States government

NM_005295.3(GPR22):c.46A>G (p.Asn16Asp) AND not specified

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Jun 16, 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:
RCV004632470.1

Allele description [Variation Report for NM_005295.3(GPR22):c.46A>G (p.Asn16Asp)]

NM_005295.3(GPR22):c.46A>G (p.Asn16Asp)

Genes:
GPR22:G protein-coupled receptor 22 [Gene - OMIM - HGNC]
COG5:component of oligomeric golgi complex 5 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
7q22.3
Genomic location:
Preferred name:
NM_005295.3(GPR22):c.46A>G (p.Asn16Asp)
HGVS:
  • NC_000007.14:g.107474106A>G
  • NG_028095.2:g.95409T>C
  • NM_001161520.2:c.538+53131T>C
  • NM_001379511.1:c.538+53131T>C
  • NM_001379512.1:c.538+53131T>C
  • NM_001379513.1:c.538+53131T>C
  • NM_001379514.1:c.538+53131T>C
  • NM_001379515.1:c.538+53131T>C
  • NM_001379516.1:c.234+83870T>C
  • NM_005295.3:c.46A>GMANE SELECT
  • NM_006348.5:c.538+53131T>CMANE SELECT
  • NM_181733.4:c.538+53131T>C
  • NP_005286.2:p.Asn16Asp
  • NC_000007.13:g.107114551A>G
  • NM_005295.2:c.46A>G
Protein change:
N16D
Molecular consequence:
  • NM_001161520.2:c.538+53131T>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001379511.1:c.538+53131T>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001379512.1:c.538+53131T>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001379513.1:c.538+53131T>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001379514.1:c.538+53131T>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001379515.1:c.538+53131T>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001379516.1:c.234+83870T>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_006348.5:c.538+53131T>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_181733.4:c.538+53131T>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_005295.3:c.46A>G - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:
AllHighlyPenetrant
Identifiers:
MedGen: CN169374

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
SCV005126184Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)		Uncertain significance
(Jun 16, 2024) 		germlineclinical testing

Citation Link

Help

Summary from all submissions

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

Details of each submission

From Ambry Genetics, SCV005126184.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided

Description

The c.46A>G (p.N16D) alteration is located in exon 3 (coding exon 1) of the GPR22 gene. This alteration results from a A to G substitution at nucleotide position 46, causing the asparagine (N) at amino acid position 16 to be replaced by an aspartic acid (D). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.

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

Last Updated: Sep 1, 2024