chr11-1923406-A-T

Position:

• chr11-1923406-A-T

Variant summary

Our verdict is Benign. Variant got -20 ACMG points: 0P and 20B. BP4_Strong BP6_Very_Strong BA1

The NM_006757.4(TNNT3):​c.32-149A>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.81 in 880,404 control chromosomes in the GnomAD database, including 291,443 homozygotes. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Benign (★★).

• Frequency:
  • Genomes: 𝑓 0.77 (45428 hom., cov: 27)
  • Exomes 𝑓: 0.82 (246015 hom.)
• Consequence: TNNT3 NM_006757.4 intron
• Clinical Significance: Benign criteria provided, multiple submitters, no conflicts B:3 O:1
• Conservation: PhyloP100: -1.69

Genes affected

TNNT3 (HGNC:11950): (troponin T3, fast skeletal type) The binding of Ca(2+) to the trimeric troponin complex initiates the process of muscle contraction. Increased Ca(2+) concentrations produce a conformational change in the troponin complex that is transmitted to tropomyosin dimers situated along actin filaments. The altered conformation permits increased interaction between a myosin head and an actin filament which, ultimately, produces a muscle contraction. The troponin complex has protein subunits C, I, and T. Subunit C binds Ca(2+) and subunit I binds to actin and inhibits actin-myosin interaction. Subunit T binds the troponin complex to the tropomyosin complex and is also required for Ca(2+)-mediated activation of actomyosin ATPase activity. There are 3 different troponin T genes that encode tissue-specific isoforms of subunit T for fast skeletal-, slow skeletal-, and cardiac-muscle. This gene encodes fast skeletal troponin T protein; also known as troponin T type 3. Alternative splicing results in multiple transcript variants encoding additional distinct troponin T type 3 isoforms. A developmentally regulated switch between fetal/neonatal and adult troponin T type 3 isoforms occurs. Additional splice variants have been described but their biological validity has not been established. Mutations in this gene may cause distal arthrogryposis multiplex congenita type 2B (DA2B). [provided by RefSeq, Oct 2009]

ACMG classification

Verdict is Benign. Variant got -20 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.94).
• BP6: Variant 11-1923406-A-T is Benign according to our data. Variant chr11-1923406-A-T is described in ClinVar as [Benign]. Clinvar id is 31869.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars.
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.908 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
TNNT3	NM_006757.4	c.32-149A>T		intron_variant		ENST00000278317.11

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
TNNT3	ENST00000278317.11	c.32-149A>T		intron_variant		5	NM_006757.4	A2

Frequencies

GnomAD3 genomes AF: 0.770 AC: 116502 AN: 151288 Hom.: 45411 Cov.: 27

Gnomad AFR AF: 0.638

Gnomad AMI AF: 0.808

Gnomad AMR AF: 0.847

Gnomad ASJ AF: 0.858

Gnomad EAS AF: 0.930

Gnomad SAS AF: 0.916

Gnomad FIN AF: 0.767

Gnomad MID AF: 0.883

Gnomad NFE AF: 0.804

Gnomad OTH AF: 0.791

GnomAD4 exome AF: 0.819 AC: 596995 AN: 728998 Hom.: 246015 AF XY: 0.824 AC XY: 317419 AN XY: 385136

Gnomad4 AFR exome AF: 0.631

Gnomad4 AMR exome AF: 0.885

Gnomad4 ASJ exome AF: 0.854

Gnomad4 EAS exome AF: 0.929

Gnomad4 SAS exome AF: 0.913

Gnomad4 FIN exome AF: 0.766

Gnomad4 NFE exome AF: 0.802

Gnomad4 OTH exome AF: 0.814

GnomAD4 genome AF: 0.770 AC: 116563 AN: 151406 Hom.: 45428 Cov.: 27 AF XY: 0.773 AC XY: 57195 AN XY: 73958

Gnomad4 AFR AF: 0.638

Gnomad4 AMR AF: 0.847

Gnomad4 ASJ AF: 0.858

Gnomad4 EAS AF: 0.930

Gnomad4 SAS AF: 0.916

Gnomad4 FIN AF: 0.767

Gnomad4 NFE AF: 0.804

Gnomad4 OTH AF: 0.787

Alfa AF: 0.777 Hom.: 5445

Bravo AF: 0.766

Asia WGS AF: 0.860 AC: 2990 AN: 3478

ClinVar

Significance: Benign

Submissions summary: Benign:3 Other:1

Revision: criteria provided, multiple submitters, no conflicts

Submissions by phenotype

not provided Benign:2 Other:1

Benign, criteria provided, single submitter	clinical testing	GeneDx	Nov 12, 2018	- -
Benign, criteria provided, single submitter	not provided	Breakthrough Genomics, Breakthrough Genomics	-	- -
not provided, no classification provided	curation	Leiden Muscular Dystrophy (TNNT3)	Mar 18, 2012	- -

Arthrogryposis, distal, type 2B2 Benign:1

Benign, criteria provided, single submitter

clinical testing

Genome-Nilou Lab

Jul 14, 2021

- -

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.94
CADD	Benign	0.63
DANN	Benign	0.75

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: rs2734500; hg19: chr11-1944636;