chr18-3457778-T-G

Variant names:

Variant summary

Our verdict is Benign. The variant received -21 ACMG points: 0P and 21B. BP4_StrongBP6_Very_StrongBP7BA1

The NM_003244.4(TGIF1):c.657T>G(p.Thr219Thr) variant causes a synonymous change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0147 in 1,613,990 control chromosomes in the GnomAD database, including 1,204 homozygotes. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Likely benign (★★).

Frequency

Genomes: 𝑓 0.052 ( 562 hom., cov: 32)

Exomes 𝑓: 0.011 ( 642 hom. )

Consequence

TGIF1
NM_003244.4 synonymous

Scores

Clinical Significance

Benign/Likely benign criteria provided, multiple submitters, no conflicts B:5

Conservation

PhyloP100: -5.48

Publications

9 publications found

Variant links:

Genes affected

TGIF1 (HGNC:11776): (TGFB induced factor homeobox 1) The protein encoded by this gene is a member of the three-amino acid loop extension (TALE) superclass of atypical homeodomains. TALE homeobox proteins are highly conserved transcription regulators. This particular homeodomain binds to a previously characterized retinoid X receptor responsive element from the cellular retinol-binding protein II promoter. In addition to its role in inhibiting 9-cis-retinoic acid-dependent RXR alpha transcription activation of the retinoic acid responsive element, the protein is an active transcriptional co-repressor of SMAD2 and may participate in the transmission of nuclear signals during development and in the adult. Mutations in this gene are associated with holoprosencephaly type 4, which is a structural anomaly of the brain. Alternative splicing has been observed at this locus and multiple splice variants encoding distinct isoforms are described. [provided by RefSeq, Jul 2013]

TGIF1 Gene-Disease associations (from GenCC):

holoprosencephaly 4
Inheritance: AD Classification: DEFINITIVE, STRONG, LIMITED Submitted by: Laboratory for Molecular Medicine, Labcorp Genetics (formerly Invitae), G2P, Ambry Genetics

TGIF1 links:

Genome browser will be placed here

ACMG classification

Classification was made for transcript

Our verdict: Benign. The variant received -21 ACMG points.

BP4

Computational evidence support a benign effect (BayesDel_noAF=-1.05).

BP6

Variant 18-3457778-T-G is Benign according to our data. Variant chr18-3457778-T-G is described in CliVar as Benign/Likely_benign. Clinvar id is 259019.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr18-3457778-T-G is described in CliVar as Benign/Likely_benign. Clinvar id is 259019.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr18-3457778-T-G is described in CliVar as Benign/Likely_benign. Clinvar id is 259019.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr18-3457778-T-G is described in CliVar as Benign/Likely_benign. Clinvar id is 259019.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr18-3457778-T-G is described in CliVar as Benign/Likely_benign. Clinvar id is 259019.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr18-3457778-T-G is described in CliVar as Benign/Likely_benign. Clinvar id is 259019.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr18-3457778-T-G is described in CliVar as Benign/Likely_benign. Clinvar id is 259019.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr18-3457778-T-G is described in CliVar as Benign/Likely_benign. Clinvar id is 259019.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr18-3457778-T-G is described in CliVar as Benign/Likely_benign. Clinvar id is 259019.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr18-3457778-T-G is described in CliVar as Benign/Likely_benign. Clinvar id is 259019.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr18-3457778-T-G is described in CliVar as Benign/Likely_benign. Clinvar id is 259019.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr18-3457778-T-G is described in CliVar as Benign/Likely_benign. Clinvar id is 259019.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr18-3457778-T-G is described in CliVar as Benign/Likely_benign. Clinvar id is 259019.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr18-3457778-T-G is described in CliVar as Benign/Likely_benign. Clinvar id is 259019.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr18-3457778-T-G is described in CliVar as Benign/Likely_benign. Clinvar id is 259019.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr18-3457778-T-G is described in CliVar as Benign/Likely_benign. Clinvar id is 259019.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr18-3457778-T-G is described in CliVar as Benign/Likely_benign. Clinvar id is 259019.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr18-3457778-T-G is described in CliVar as Benign/Likely_benign. Clinvar id is 259019.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr18-3457778-T-G is described in CliVar as Benign/Likely_benign. Clinvar id is 259019.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr18-3457778-T-G is described in CliVar as Benign/Likely_benign. Clinvar id is 259019.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr18-3457778-T-G is described in CliVar as Benign/Likely_benign. Clinvar id is 259019.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr18-3457778-T-G is described in CliVar as Benign/Likely_benign. Clinvar id is 259019.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr18-3457778-T-G is described in CliVar as Benign/Likely_benign. Clinvar id is 259019.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr18-3457778-T-G is described in CliVar as Benign/Likely_benign. Clinvar id is 259019.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr18-3457778-T-G is described in CliVar as Benign/Likely_benign. Clinvar id is 259019.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr18-3457778-T-G is described in CliVar as Benign/Likely_benign. Clinvar id is 259019.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr18-3457778-T-G is described in CliVar as Benign/Likely_benign. Clinvar id is 259019.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr18-3457778-T-G is described in CliVar as Benign/Likely_benign. Clinvar id is 259019.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr18-3457778-T-G is described in CliVar as Benign/Likely_benign. Clinvar id is 259019.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars. Variant chr18-3457778-T-G is described in CliVar as Benign/Likely_benign. Clinvar id is 259019.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars.

BP7

Synonymous conserved (PhyloP=-5.48 with no splicing effect.

BA1

GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.16 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
TGIF1	NM_003244.4 link	c.657T>G	p.Thr219Thr	synonymous_variant	Exon 3 of 3	ENST00000343820.10	NP_003235.1	Q15583-2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
TGIF1	ENST00000343820.10 link	c.657T>G	p.Thr219Thr	synonymous_variant	Exon 3 of 3	1	NM_003244.4	ENSP00000339631.6		Q15583-2

Frequencies

GnomAD3 genomes

AF:

0.0522

AC:

7939

AN:

152090

Hom.:

556

Cov.:

show subpopulations

Gnomad AFR

AF:

0.163

Gnomad AMI

AF:

0.0219

Gnomad AMR

AF:

0.0280

Gnomad ASJ

AF:

0.0196

Gnomad EAS

AF:

0.00115

Gnomad SAS

AF:

0.00393

Gnomad FIN

AF:

0.00735

Gnomad MID

AF:

0.0443

Gnomad NFE

AF:

0.00641

Gnomad OTH

AF:

0.0542

GnomAD2 exomes

AF:

0.0190

AC:

4764

AN:

251380

AF XY:

0.0156

show subpopulations

Gnomad AFR exome

AF:

0.170

Gnomad AMR exome

AF:

0.0176

Gnomad ASJ exome

AF:

0.0194

Gnomad EAS exome

AF:

0.00120

Gnomad FIN exome

AF:

0.00738

Gnomad NFE exome

AF:

0.00669

Gnomad OTH exome

AF:

0.0215

GnomAD4 exome

AF:

0.0108

AC:

15737

AN:

1461782

Hom.:

642

Cov.:

AF XY:

0.0102

AC XY:

7389

AN XY:

727212

show subpopulations

African (AFR)

AF:

0.174

AC:

5835

AN:

33480

American (AMR)

AF:

0.0191

AC:

856

AN:

44724

Ashkenazi Jewish (ASJ)

AF:

0.0207

AC:

542

AN:

26136

East Asian (EAS)

AF:

0.000479

AC:

AN:

39700

South Asian (SAS)

AF:

0.00442

AC:

381

AN:

86258

European-Finnish (FIN)

AF:

0.00829

AC:

442

AN:

53312

Middle Eastern (MID)

AF:

0.0374

AC:

216

AN:

5768

European-Non Finnish (NFE)

AF:

0.00549

AC:

6107

AN:

1112008

Other (OTH)

AF:

0.0222

AC:

1339

AN:

60396

Allele Balance Distribution

Red line indicates average allele balance

Average allele balance: 0.478

Heterozygous variant carriers

1039

2078

3117

4156

5195

0.00

0.20

0.40

0.60

0.80

0.95

Allele balance

Age Distribution

Exome Het

Exome Hom

Variant carriers

332

664

996

1328

1660

<30

30-35

35-40

40-45

45-50

50-55

55-60

60-65

65-70

70-75

75-80

>80

Age

GnomAD4 genome

AF:

0.0523

AC:

7967

AN:

152208

Hom.:

562

Cov.:

AF XY:

0.0507

AC XY:

3773

AN XY:

74432

show subpopulations

African (AFR)

AF:

0.164

AC:

6787

AN:

41484

American (AMR)

AF:

0.0279

AC:

427

AN:

15294

Ashkenazi Jewish (ASJ)

AF:

0.0196

AC:

AN:

3472

East Asian (EAS)

AF:

0.00116

AC:

AN:

5186

South Asian (SAS)

AF:

0.00373

AC:

AN:

4828

European-Finnish (FIN)

AF:

0.00735

AC:

AN:

10618

Middle Eastern (MID)

AF:

0.0476

AC:

AN:

294

European-Non Finnish (NFE)

AF:

0.00641

AC:

436

AN:

68012

Other (OTH)

AF:

0.0536

AC:

113

AN:

2108

Allele Balance Distribution

Red line indicates average allele balance

Average allele balance: 0.502

Heterozygous variant carriers

342

685

1027

1370

1712

0.00

0.20

0.40

0.60

0.80

0.95

Allele balance

Age Distribution

Genome Het

Genome Hom

Variant carriers

148

222

296

370

<30

30-35

35-40

40-45

45-50

50-55

55-60

60-65

65-70

70-75

75-80

>80

Age

Alfa

AF:

0.0298

Hom.:

192

Bravo

AF:

0.0602

Asia WGS

AF:

0.0200

AC:

AN:

3478

EpiCase

AF:

0.00725

EpiControl

AF:

0.00830

ClinVar

Significance: Benign/Likely benign

Submissions summary: Benign:5

Revision: criteria provided, multiple submitters, no conflicts

LINK: link

Submissions by phenotype

not provided

Benign:2

Mar 03, 2015

GeneDx

Significance: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:1

PreventionGenetics, part of Exact Sciences

Significance:Benign

Review Status:criteria provided, single submitter

Collection Method:clinical testing

- -

Holoprosencephaly 4

Benign:1

Feb 03, 2025

Labcorp Genetics (formerly Invitae), Labcorp

Significance:Benign

Review Status:criteria provided, single submitter

Collection Method:clinical testing

- -

Holoprosencephaly sequence

Benign:1

Jun 14, 2016

Illumina Laboratory Services, Illumina

Significance:Likely benign

Review Status:criteria provided, single submitter

Collection Method:clinical testing

- -

Computational scores

Source: dbNSFP v4.3

Name

Calibrated prediction

Score

Prediction

BayesDel_noAF

Benign

-1.1

CADD

Benign

0.070

(source)

DANN

Benign

0.19

PhyloP100

-5.5

Mutation Taster

=100/0

polymorphism (auto)

(source)

Splicing

Name

Calibrated prediction

Score

Prediction

SpliceAI score (max)

0.010

Details are displayed if max score is > 0.2

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

Publications

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Variant summary

Frequency

Consequence

Scores

Clinical Significance

Conservation

Publications

ACMG classification

Transcripts

RefSeq

Ensembl

Frequencies

Age Distribution

Age Distribution

ClinVar

Submissions by phenotype

Computational scores

Splicing

Publications

Other links and lift over