NM_201525.4(ADGRG1):c.14C>T (p.Ser5Leu) AND Bilateral frontoparietal polymicrogyria

Germline classification:: Uncertain significance (2 submissions)
Last evaluated:: Mar 2, 2018
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:: RCV001116136.6

Allele description [Variation Report for NM_201525.4(ADGRG1):c.14C>T (p.Ser5Leu)]

NM_201525.4(ADGRG1):c.14C>T (p.Ser5Leu)

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.14C>T (p.Ser5Leu)

HGVS:

NC_000016.10:g.57650301C>T
NG_011643.1:g.35304C>T
NM_001145770.3:c.14C>T
NM_001145771.3:c.14C>T
NM_001145772.3:c.14C>T
NM_001145773.3:c.14C>T
NM_001145774.3:c.14C>T
NM_001290142.2:c.14C>T
NM_001290143.2:c.-469C>T
NM_001290144.2:c.-469C>T
NM_001370428.1:c.14C>T
NM_001370429.1:c.14C>T
NM_001370430.1:c.14C>T
NM_001370431.1:c.14C>T
NM_001370432.1:c.14C>T
NM_001370433.1:c.14C>T
NM_001370434.1:c.14C>T
NM_001370435.1:c.14C>T
NM_001370436.1:c.14C>T
NM_001370437.1:c.14C>T
NM_001370438.1:c.14C>T
NM_001370439.1:c.14C>T
NM_001370440.1:c.14C>T
NM_001370441.1:c.14C>T
NM_001370442.1:c.14C>T
NM_001370451.1:c.-469C>T
NM_001370453.1:c.-553C>T
NM_001370454.1:c.-414-946C>T
NM_005682.7:c.14C>T
NM_201524.4:c.14C>T
NM_201525.4:c.14C>TMANE SELECT
NP_001139242.1:p.Ser5Leu
NP_001139243.1:p.Ser5Leu
NP_001139244.1:p.Ser5Leu
NP_001139245.1:p.Ser5Leu
NP_001139246.1:p.Ser5Leu
NP_001277071.1:p.Ser5Leu
NP_001357357.1:p.Ser5Leu
NP_001357358.1:p.Ser5Leu
NP_001357359.1:p.Ser5Leu
NP_001357360.1:p.Ser5Leu
NP_001357361.1:p.Ser5Leu
NP_001357362.1:p.Ser5Leu
NP_001357363.1:p.Ser5Leu
NP_001357364.1:p.Ser5Leu
NP_001357365.1:p.Ser5Leu
NP_001357366.1:p.Ser5Leu
NP_001357367.1:p.Ser5Leu
NP_001357368.1:p.Ser5Leu
NP_001357369.1:p.Ser5Leu
NP_001357370.1:p.Ser5Leu
NP_001357371.1:p.Ser5Leu
NP_005673.3:p.Ser5Leu
NP_958932.1:p.Ser5Leu
NP_958933.1:p.Ser5Leu
NC_000016.9:g.57684213C>T
NM_005682.5:c.14C>T

Protein change:

S5L

Links:

dbSNP: rs147879224

NCBI 1000 Genomes Browser:

rs147879224

Molecular consequence:

NM_001290143.2:c.-469C>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001290144.2:c.-469C>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001370451.1:c.-469C>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001370453.1:c.-553C>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001370454.1:c.-414-946C>T - intron variant - [Sequence Ontology: SO:0001627]
NM_001145770.3:c.14C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001145771.3:c.14C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001145772.3:c.14C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001145773.3:c.14C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001145774.3:c.14C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001290142.2:c.14C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001370428.1:c.14C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001370429.1:c.14C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001370430.1:c.14C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001370431.1:c.14C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001370432.1:c.14C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001370433.1:c.14C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001370434.1:c.14C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001370435.1:c.14C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001370436.1:c.14C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001370437.1:c.14C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001370438.1:c.14C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001370439.1:c.14C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001370440.1:c.14C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001370441.1:c.14C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001370442.1:c.14C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_005682.7:c.14C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_201524.4:c.14C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_201525.4:c.14C>T - missense variant - [Sequence Ontology: SO:0001583]

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

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001274172	Illumina Laboratory Services, Illumina	criteria provided, single submitter (ICSL Variant Classification Criteria 13 December 2019)	Uncertain significance (Mar 2, 2018)	germline	clinical testing	Citation Link,
SCV001462688	Natera, Inc.	no assertion criteria provided	Uncertain significance (Jan 17, 2020)	germline	clinical testing

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV001274172

Illumina Laboratory Services, Illumina

criteria provided, single submitter

(ICSL Variant Classification Criteria 13 December 2019)

Uncertain significance
(Mar 2, 2018)

germline

clinical testing

Citation Link,

SCV001462688

Natera, Inc.

no assertion criteria provided

Uncertain significance
(Jan 17, 2020)

germline

clinical testing

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

Details of each submission

From Illumina Laboratory Services, Illumina, SCV001274172.1

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

Description

This variant was observed in the ICSL laboratory as part of a predisposition screen in an ostensibly healthy population. It had not been previously curated by ICSL or reported in the Human Gene Mutation Database (HGMD: prior to June 1st, 2018), and was therefore a candidate for classification through an automated scoring system. Utilizing variant allele frequency, disease prevalence and penetrance estimates, and inheritance mode, an automated score was calculated to assess if this variant is too frequent to cause the disease. Based on the score, this variant could not be ruled out of causing disease and therefore its association with disease required further investigation. A literature search was performed for the gene, cDNA change, and amino acid change (if applicable). No publications were found based on this search. This variant was therefore classified as a variant of unknown significance for this disease.

#	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

From Natera, Inc., SCV001462688.1

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

#	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

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