NM_001374353.1:c.3892C>T

Variant names:

Variant summary

Our verdict is Benign. Variant got -20 ACMG points: 0P and 20B. BP4_StrongBP6_Very_StrongBS1BS2

The NM_001374353.1(GLI2):c.3892C>T(p.Pro1298Ser) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0242 in 1,612,970 control chromosomes in the GnomAD database, including 588 homozygotes. In-silico tool predicts a benign outcome for this variant. 14/20 in silico tools predict a benign outcome for this variant. Variant has been reported in ClinVar as Likely benign (★★).

Frequency

Genomes: 𝑓 0.017 ( 35 hom., cov: 33)

Exomes 𝑓: 0.025 ( 553 hom. )

Consequence

GLI2
NM_001374353.1 missense

Scores

Clinical Significance

Benign/Likely benign criteria provided, multiple submitters, no conflicts B:8

Conservation

PhyloP100: -0.0310

Variant links:

Genes affected

GLI2 (HGNC:4318): (GLI family zinc finger 2) This gene encodes a protein which belongs to the C2H2-type zinc finger protein subclass of the Gli family. Members of this subclass are characterized as transcription factors which bind DNA through zinc finger motifs. These motifs contain conserved H-C links. Gli family zinc finger proteins are mediators of Sonic hedgehog (Shh) signaling and they are implicated as potent oncogenes in the embryonal carcinoma cell. The protein encoded by this gene localizes to the cytoplasm and activates patched Drosophila homolog (PTCH) gene expression. It is also thought to play a role during embryogenesis. The encoded protein is associated with several phenotypes- Greig cephalopolysyndactyly syndrome, Pallister-Hall syndrome, preaxial polydactyly type IV, postaxial polydactyly types A1 and B. [provided by RefSeq, Jul 2008]

GLI2 links:

Genome browser will be placed here

ACMG classification

Classification made for transcript

Verdict is Benign. Variant got -20 ACMG points.

BP4

Computational evidence support a benign effect (MetaRNN=0.0033062696).

BP6

Variant 2-120989857-C-T is Benign according to our data. Variant chr2-120989857-C-T is described in ClinVar as [Likely_benign]. Clinvar id is 95274.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr2-120989857-C-T is described in Lovd as [Likely_benign].

BS1

Variant frequency is greater than expected in population nfe. gnomad4 allele frequency = 0.0168 (2562/152358) while in subpopulation NFE AF= 0.0275 (1870/68018). AF 95% confidence interval is 0.0265. There are 35 homozygotes in gnomad4. There are 1176 alleles in male gnomad4 subpopulation. Median coverage is 33. This position pass quality control queck.

BS2

High AC in GnomAd4 at 2562 AD gene.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
GLI2	NM_001374353.1 link	c.3892C>T	p.Pro1298Ser	missense_variant	Exon 14 of 14	ENST00000361492.9	NP_001361282.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
GLI2	ENST00000361492.9 link	c.3892C>T	p.Pro1298Ser	missense_variant	Exon 14 of 14	1	NM_001374353.1	ENSP00000354586.5		A0A7I2PJA1

Frequencies

GnomAD3 genomes

AF:

0.0168

AC:

2563

AN:

152240

Hom.:

Cov.:

show subpopulations

Gnomad AFR

AF:

0.00453

Gnomad AMI

AF:

0.00

Gnomad AMR

AF:

0.0165

Gnomad ASJ

AF:

0.00778

Gnomad EAS

AF:

0.000961

Gnomad SAS

AF:

0.0195

Gnomad FIN

AF:

0.00725

Gnomad MID

AF:

0.00633

Gnomad NFE

AF:

0.0275

Gnomad OTH

AF:

0.0220

GnomAD3 exomes

AF:

0.0163

AC:

4054

AN:

248274

Hom.:

AF XY:

0.0168

AC XY:

2270

AN XY:

134916

show subpopulations

Gnomad AFR exome

AF:

0.00386

Gnomad AMR exome

AF:

0.0110

Gnomad ASJ exome

AF:

0.00812

Gnomad EAS exome

AF:

0.000110

Gnomad SAS exome

AF:

0.0152

Gnomad FIN exome

AF:

0.00715

Gnomad NFE exome

AF:

0.0252

Gnomad OTH exome

AF:

0.0159

GnomAD4 exome

AF:

0.0249

AC:

36430

AN:

1460612

Hom.:

553

Cov.:

AF XY:

0.0246

AC XY:

17889

AN XY:

726606

show subpopulations

Gnomad4 AFR exome

AF:

0.00281

Gnomad4 AMR exome

AF:

0.0107

Gnomad4 ASJ exome

AF:

0.00896

Gnomad4 EAS exome

AF:

0.000151

Gnomad4 SAS exome

AF:

0.0159

Gnomad4 FIN exome

AF:

0.00811

Gnomad4 NFE exome

AF:

0.0291

Gnomad4 OTH exome

AF:

0.0224

GnomAD4 genome

AF:

0.0168

AC:

2562

AN:

152358

Hom.:

Cov.:

AF XY:

0.0158

AC XY:

1176

AN XY:

74508

show subpopulations

Gnomad4 AFR

AF:

0.00452

Gnomad4 AMR

AF:

0.0165

Gnomad4 ASJ

AF:

0.00778

Gnomad4 EAS

AF:

0.000963

Gnomad4 SAS

AF:

0.0195

Gnomad4 FIN

AF:

0.00725

Gnomad4 NFE

AF:

0.0275

Gnomad4 OTH

AF:

0.0218

Alfa

AF:

0.0243

Hom.:

Bravo

AF:

0.0161

TwinsUK

AF:

0.0200

AC:

ALSPAC

AF:

0.0246

AC:

ESP6500AA

AF:

0.00341

AC:

ESP6500EA

AF:

0.0267

AC:

230

ExAC

AF:

0.0162

AC:

1971

Asia WGS

AF:

0.00491

AC:

AN:

3478

EpiCase

AF:

0.0262

EpiControl

AF:

0.0251

ClinVar

Significance: Benign/Likely benign

Submissions summary: Benign:8

Revision: criteria provided, multiple submitters, no conflicts

LINK: link

Submissions by phenotype

not provided

Benign:4

Mar 01, 2025

CeGaT Center for Human Genetics Tuebingen

Significance: Benign

Review Status: criteria provided, single submitter

Collection Method: clinical testing

GLI2: BP4, BS1, BS2 -

Mar 09, 2021

GeneDx

Significance: Benign

Review Status: criteria provided, single submitter

Collection Method: clinical testing

This variant is associated with the following publications: (PMID: 19223936, 24744436, 29260090, 22967285) -

Nov 01, 2023

ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

Significance: Likely benign

Review Status: criteria provided, single submitter

Collection Method: clinical testing

- -

Breakthrough Genomics, Breakthrough Genomics

Significance: Likely benign

Review Status: criteria provided, single submitter

Collection Method: not provided

- -

not specified

Benign:2

PreventionGenetics, part of Exact Sciences

Significance: Likely benign

Review Status: criteria provided, single submitter

Collection Method: clinical testing

- -

Aug 13, 2013

Eurofins Ntd Llc (ga)

Significance: Benign

Review Status: criteria provided, single submitter

Collection Method: clinical testing

- -

Holoprosencephaly 9;C4014479:Postaxial polydactyly-anterior pituitary anomalies-facial dysmorphism syndrome

Benign:1

Feb 02, 2025

Labcorp Genetics (formerly Invitae), Labcorp

Significance: Benign

Review Status: criteria provided, single submitter

Collection Method: clinical testing

- -

Holoprosencephaly 9

Benign:1

Jan 13, 2018

Illumina Laboratory Services, Illumina

Significance: Benign

Review Status: criteria provided, single submitter

Collection Method: clinical testing

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 and internal cut-off values, a variant classified as benign is not then subjected to further curation. The score for this variant resulted in a classification of benign for this disease. -

Computational scores

Source: dbNSFP v4.3

Name

Calibrated prediction

Score

Prediction

AlphaMissense

Benign

0.061

BayesDel_addAF

Benign

-0.72

BayesDel_noAF

Benign

-0.79

CADD

Benign

3.0

DANN

Benign

0.24

DEOGEN2

Benign

0.29

T;T

Eigen

Benign

-0.86

Eigen_PC

Benign

-0.87

FATHMM_MKL

Benign

0.10

LIST_S2

Benign

0.60

.;T

MetaRNN

Benign

0.0033

T;T

MetaSVM

Benign

-0.97

MutationAssessor

Benign

0.90

L;L

PrimateAI

Benign

0.28

PROVEAN

Benign

-1.1

N;N

REVEL

Benign

0.017

Sift

Benign

0.65

T;T

Sift4G

Benign

0.42

T;T

Polyphen

0.0010

B;B

Vest4

0.029

MPC

0.33

ClinPred

0.0016

GERP RS

1.0

Varity_R

0.067

gMVP

0.13

Splicing

Name

Calibrated prediction

Score

Prediction

SpliceAI score (max)

0.0

Details are displayed if max score is > 0.2

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Publications

LitVar

Below is the list of publications found by LitVar. It may be empty.

Variant summary

Frequency

Consequence

Scores

Clinical Significance

Conservation

ACMG classification

Transcripts

RefSeq

Ensembl

Frequencies

ClinVar

Submissions by phenotype

Computational scores

Splicing

Publications

LitVar

Other links and lift over