Variant chr10-112951514-G-T details in Genebe, Genetics Data Aggregator

Variant summary

Our verdict is Uncertain significance. Variant got 2 ACMG points: 2P and 0B. PM2

The NM_001367943.1(TCF7L2):c.288G>T(p.Lys96Asn) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. Variant has been reported in ClinVar as Uncertain significance (★).

Frequency

Genomes: not found (cov: 29)

Exomes 𝑓: 0.0 ( 0 hom. )

Failed GnomAD Quality Control

Consequence

TCF7L2
NM_001367943.1 missense

Scores

Clinical Significance

Uncertain significance criteria provided, single submitter U:1

Conservation

PhyloP100: 3.36

Variant links:

Genes affected

TCF7L2 (HGNC:11641): (transcription factor 7 like 2) This gene encodes a high mobility group (HMG) box-containing transcription factor that plays a key role in the Wnt signaling pathway. The protein has been implicated in blood glucose homeostasis. Genetic variants of this gene are associated with increased risk of type 2 diabetes. Several transcript variants encoding multiple different isoforms have been found for this gene.[provided by RefSeq, Oct 2010]

TCF7L2 links:

(HGNC:):

links:

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ACMG classification

Classification made for transcript

Verdict is Uncertain_significance. Variant got 2 ACMG points.

PM2

Very rare variant in population databases, with high coverage;

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
TCF7L2	NM_001367943.1 linkuse as main transcript	c.288G>T	p.Lys96Asn	missense_variant	3/15	ENST00000355995.9
LOC124902502	XR_007062291.1 linkuse as main transcript	n.565+264C>A		intron_variant, non_coding_transcript_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
TCF7L2	ENST00000355995.9 linkuse as main transcript	c.288G>T	p.Lys96Asn	missense_variant	3/15	1	NM_001367943.1		Q9NQB0-1
	ENST00000369391.3 linkuse as main transcript	n.98+264C>A		intron_variant, non_coding_transcript_variant		3

Frequencies

GnomAD3 genomes

Cov.:

GnomAD4 exome

Data not reliable, filtered out with message: AC0

AF:

0.00

AC:

AN:

1282112

Hom.:

Cov.:

AF XY:

0.00

AC XY:

AN XY:

638580

Gnomad4 AFR exome

AF:

0.00

Gnomad4 AMR exome

AF:

0.00

Gnomad4 ASJ exome

AF:

0.00

Gnomad4 EAS exome

AF:

0.00

Gnomad4 SAS exome

AF:

0.00

Gnomad4 FIN exome

AF:

0.00

Gnomad4 NFE exome

AF:

0.00

Gnomad4 OTH exome

AF:

0.00

GnomAD4 genome

Cov.:

ClinVar

Significance: Uncertain significance

Submissions summary: Uncertain:1

Revision: criteria provided, single submitter

LINK: link

Submissions by phenotype

Intellectual disability

Uncertain:1

Uncertain significance, criteria provided, single submitter

curation

Broad Center for Mendelian Genomics, Broad Institute of MIT and Harvard

Dec 21, 2023

The heterozygous p.Lys96Asn variant in TCF7L2 was identified by our study in 1 individual with severe intellectual disability and severe scoliosis. While this gene is still lacking sufficient evidence to establish a gene-disease relationship, we believe this is a possible novel gene candidate for severe intellectual disability and severe scoliosis. Given the limited information about this gene-disease relationship, the significance of the p.Lys96Asn variant is uncertain. If you have any additional information about functional evidence or other individuals with this phenotype that also have variants in TCF7L2 we encourage you to reach out to us. -

Computational scores

Source: dbNSFP v4.3

Name

Calibrated prediction

Score

Prediction

AlphaMissense

Pathogenic

0.97

BayesDel_addAF

Pathogenic

0.18

BayesDel_noAF

Uncertain

0.020

CADD

Uncertain

DANN

Uncertain

0.99

DEOGEN2

Benign

0.082

T;T;T;.;T;.;.;.;.;T;.;T;T

Eigen

Benign

-0.091

Eigen_PC

Benign

-0.17

FATHMM_MKL

Benign

0.41

LIST_S2

Uncertain

0.92

D;D;D;D;D;D;D;D;D;D;D;D;D

M_CAP

Pathogenic

0.98

MetaRNN

Uncertain

0.69

D;D;D;D;D;D;D;D;D;D;D;D;D

MetaSVM

Pathogenic

1.1

MutationAssessor

Uncertain

2.5

.;.;M;M;.;M;M;M;M;.;.;.;.

MutationTaster

Benign

0.98

D;D;D;D;D;D;D;D;D;D;D;D

PrimateAI

Pathogenic

0.89

PROVEAN

Uncertain

-2.5

D;D;D;N;D;.;D;D;D;D;D;.;D

REVEL

Pathogenic

0.66

Sift

Uncertain

0.0020

D;D;D;D;D;.;D;D;D;D;D;.;D

Sift4G

Benign

0.14

T;D;D;T;D;D;D;T;T;D;T;D;D

Polyphen

0.15, 0.053, 0.58

.;B;.;.;.;B;.;.;.;.;P;.;.

Vest4

0.59

MutPred

0.50

Loss of methylation at K96 (P = 0);Loss of methylation at K96 (P = 0);Loss of methylation at K96 (P = 0);Loss of methylation at K96 (P = 0);Loss of methylation at K96 (P = 0);Loss of methylation at K96 (P = 0);Loss of methylation at K96 (P = 0);Loss of methylation at K96 (P = 0);Loss of methylation at K96 (P = 0);Loss of methylation at K96 (P = 0);Loss of methylation at K96 (P = 0);Loss of methylation at K96 (P = 0);.;

MVP

0.94

MPC

0.85

ClinPred

0.97

GERP RS

2.3

RBP_binding_hub_radar

0.0

RBP_regulation_power_radar

1.7

Varity_R

0.76

gMVP

0.48

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

No publications associated with this variant yet.

Variant summary

Frequency

Consequence

Scores

Clinical Significance

Conservation

ACMG classification

Transcripts

RefSeq

Ensembl

Frequencies

ClinVar

Submissions by phenotype

Computational scores

Splicing

Publications

Other links and lift over