NM_201525.4(ADGRG1):c.64+5G>A AND Bilateral frontoparietal polymicrogyria

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Mar 1, 2020
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:: RCV001264822.2

Allele description [Variation Report for NM_201525.4(ADGRG1):c.64+5G>A]

NM_201525.4(ADGRG1):c.64+5G>A

Gene:

ADGRG1:adhesion G protein-coupled receptor G1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

16q21

Genomic location:

Preferred name:

NM_201525.4(ADGRG1):c.64+5G>A

HGVS:

NC_000016.10:g.57650356G>A
NG_011643.1:g.35359G>A
NM_001145770.3:c.64+5G>A
NM_001145771.3:c.64+5G>A
NM_001145772.3:c.64+5G>A
NM_001145773.3:c.64+5G>A
NM_001145774.3:c.64+5G>A
NM_001290142.2:c.64+5G>A
NM_001290143.2:c.-419+5G>A
NM_001290144.2:c.-419+5G>A
NM_001370428.1:c.64+5G>A
NM_001370429.1:c.64+5G>A
NM_001370430.1:c.64+5G>A
NM_001370431.1:c.64+5G>A
NM_001370432.1:c.64+5G>A
NM_001370433.1:c.64+5G>A
NM_001370434.1:c.64+5G>A
NM_001370435.1:c.64+5G>A
NM_001370436.1:c.64+5G>A
NM_001370437.1:c.64+5G>A
NM_001370438.1:c.64+5G>A
NM_001370439.1:c.64+5G>A
NM_001370440.1:c.64+5G>A
NM_001370441.1:c.64+5G>A
NM_001370442.1:c.64+5G>A
NM_001370451.1:c.-419+5G>A
NM_001370453.1:c.-503+5G>A
NM_001370454.1:c.-414-891G>A
NM_005682.7:c.64+5G>A
NM_201524.4:c.64+5G>A
NM_201525.4:c.64+5G>AMANE SELECT
NC_000016.9:g.57684268G>A
NM_005682.5:c.64+5G>A

Links:

dbSNP: rs2043729030

NCBI 1000 Genomes Browser:

rs2043729030

Molecular consequence:

NM_001145770.3:c.64+5G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001145771.3:c.64+5G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001145772.3:c.64+5G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001145773.3:c.64+5G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001145774.3:c.64+5G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001290142.2:c.64+5G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001290143.2:c.-419+5G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001290144.2:c.-419+5G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001370428.1:c.64+5G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001370429.1:c.64+5G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001370430.1:c.64+5G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001370431.1:c.64+5G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001370432.1:c.64+5G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001370433.1:c.64+5G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001370434.1:c.64+5G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001370435.1:c.64+5G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001370436.1:c.64+5G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001370437.1:c.64+5G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001370438.1:c.64+5G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001370439.1:c.64+5G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001370440.1:c.64+5G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001370441.1:c.64+5G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001370442.1:c.64+5G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001370451.1:c.-419+5G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001370453.1:c.-503+5G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001370454.1:c.-414-891G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_005682.7:c.64+5G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_201524.4:c.64+5G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_201525.4:c.64+5G>A - intron variant - [Sequence Ontology: SO:0001627]

Condition(s)

Name:: Bilateral frontoparietal polymicrogyria
Synonyms:: CEREBELLAR ATAXIA WITH NEURONAL MIGRATION DEFECT; CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 14A (BILATERAL FRONTOPARIETAL)
Identifiers:: MONDO: MONDO:0011738; MedGen: C1847352; OMIM: 606854

Recent activity

Clear Turn Off Turn On

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
SCV001443014	Institute of Human Genetics, University of Leipzig Medical Center	criteria provided, single submitter (ACMG Guidelines, 2015)	Uncertain significance (Mar 1, 2020)	biparental	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

SCV001443014

Institute of Human Genetics, University of Leipzig Medical Center

criteria provided, single submitter

(ACMG Guidelines, 2015)

Uncertain significance
(Mar 1, 2020)

biparental

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	biparental	yes	not provided	not provided	not provided	not provided	not provided	clinical 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 Institute of Human Genetics, University of Leipzig Medical Center, SCV001443014.1

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

Description

Review of the variants reported in Reuter et al., 2017, PMID: 28097321: PM2,PM3_Supporting,(PP1)

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

Last Updated: Sep 16, 2023

ClinVar

Relating variation to medicine