rs35969244

chr18-55260169-T-C

Variant summary

Our verdict is Benign. Variant got -14 ACMG points: 0P and 14B. BP4_Strong BP6_Moderate BA1

The NM_001083962.2(TCF4):c.991-142A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0952 in 684,884 control chromosomes in the GnomAD database, including 3,672 homozygotes. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Benign (★).

• Frequency:
  • Genomes: 𝑓 0.10 (934 hom., cov: 32)
  • Exomes 𝑓: 0.093 (2738 hom.)
• Consequence: TCF4 NM_001083962.2 intron
• Clinical Significance: Benign criteria provided, single submitter B:1
• Conservation: PhyloP100: -1.02

Genes affected

TCF4 (HGNC:11634): (transcription factor 4) This gene encodes transcription factor 4, a basic helix-loop-helix transcription factor. The encoded protein recognizes an Ephrussi-box ('E-box') binding site ('CANNTG') - a motif first identified in immunoglobulin enhancers. This gene is broadly expressed, and may play an important role in nervous system development. Defects in this gene are a cause of Pitt-Hopkins syndrome. In addition, an intronic CTG repeat normally numbering 10-37 repeat units can expand to >50 repeat units and cause Fuchs endothelial corneal dystrophy. Multiple alternatively spliced transcript variants that encode different proteins have been described. [provided by RefSeq, Jul 2016]

ACMG classification

Verdict is Benign. Variant got -14 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.91).
• BP6: Variant 18-55260169-T-C is Benign according to our data. Variant chr18-55260169-T-C is described in ClinVar as [Benign]. Clinvar id is 672225.Status of the report is criteria_provided_single_submitter, 1 stars.
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.125 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
TCF4	NM_001083962.2	c.991-142A>G		intron_variant		ENST00000354452.8

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
TCF4	ENST00000354452.8	c.991-142A>G		intron_variant		5	NM_001083962.2	P3

Frequencies

GnomAD3 genomes AF: 0.102 AC: 15498 AN: 152128 Hom.: 934 Cov.: 32

Gnomad AFR AF: 0.128

Gnomad AMI AF: 0.271

Gnomad AMR AF: 0.0833

Gnomad ASJ AF: 0.186

Gnomad EAS AF: 0.00365

Gnomad SAS AF: 0.112

Gnomad FIN AF: 0.0408

Gnomad MID AF: 0.0949

Gnomad NFE AF: 0.0996

Gnomad OTH AF: 0.105

GnomAD4 exome AF: 0.0933 AC: 49689 AN: 532638 Hom.: 2738 AF XY: 0.0959 AC XY: 27637 AN XY: 288246

Gnomad4 AFR exome AF: 0.128

Gnomad4 AMR exome AF: 0.0656

Gnomad4 ASJ exome AF: 0.177

Gnomad4 EAS exome AF: 0.000767

Gnomad4 SAS exome AF: 0.118

Gnomad4 FIN exome AF: 0.0453

Gnomad4 NFE exome AF: 0.0997

Gnomad4 OTH exome AF: 0.0964

GnomAD4 genome AF: 0.102 AC: 15506 AN: 152246 Hom.: 934 Cov.: 32 AF XY: 0.0989 AC XY: 7361 AN XY: 74446

Gnomad4 AFR AF: 0.128

Gnomad4 AMR AF: 0.0831

Gnomad4 ASJ AF: 0.186

Gnomad4 EAS AF: 0.00366

Gnomad4 SAS AF: 0.111

Gnomad4 FIN AF: 0.0408

Gnomad4 NFE AF: 0.0996

Gnomad4 OTH AF: 0.104

Alfa AF: 0.0984 Hom.: 303

Bravo AF: 0.106

Asia WGS AF: 0.0600 AC: 212 AN: 3476

ClinVar

Significance: Benign

Submissions summary: Benign:1

Revision: criteria provided, single submitter

Submissions by phenotype

not provided Benign:1

Benign, criteria provided, single submitter

clinical testing

GeneDx

Jun 19, 2018

This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease. -

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.91
Cadd	Benign	0.27
Dann	Benign	0.23

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

Other links and lift over

dbSNP: rs35969244; hg19: chr18-52927400;