rs139883667

Variant names:

• chrX-124380755-G-A
• rs139883667
• ENST00000371130.7:c.7959C>T

Your query was ambiguous. Multiple possible variants found:

• chrX-124380755-G-A
• chrX-124380755-G-C

Variant summary

Our verdict is Benign. Variant got -11 ACMG points: 0P and 11B. BP4_Strong BP6_Moderate BP7 BS2

The NM_001163278.2(TENM1):​c.7980C>T​(p.Arg2660Arg) variant causes a synonymous change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.000203 in 1,209,397 control chromosomes in the GnomAD database, with no homozygous occurrence. There are 78 hemizygotes in GnomAD. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Benign (★).

• Frequency:
  • Genomes: 𝑓 0.00072 (0 hom., 17 hem., cov: 23)
  • Exomes 𝑓: 0.00015 (0 hom. 61 hem.)
• Consequence: TENM1 NM_001163278.2 synonymous
• Clinical Significance: Benign criteria provided, single submitter B:2
• Conservation: PhyloP100: -2.52

Genes affected

TENM1 (HGNC:8117): (teneurin transmembrane protein 1) The protein encoded by this gene belongs to the tenascin family and teneurin subfamily. It is expressed in the neurons and may function as a cellular signal transducer. Several alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009]

STAG2 (HGNC:11355): (STAG2 cohesin complex component) The protein encoded by this gene is a subunit of the cohesin complex, which regulates the separation of sister chromatids during cell division. Targeted inactivation of this gene results in chromatid cohesion defects and aneuploidy, suggesting that genetic disruption of cohesin is a cause of aneuploidy in human cancer. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2013]

LOC105373331 (HGNC:):

ACMG classification

Verdict is Benign. Variant got -11 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.9).
• BP6: Variant X-124380755-G-A is Benign according to our data. Variant chrX-124380755-G-A is described in ClinVar as [Benign]. Clinvar id is 786397.Status of the report is criteria_provided_single_submitter, 1 stars.
• BP7: Synonymous conserved (PhyloP=-2.52 with no splicing effect.
• BS2: High Hemizygotes in GnomAd4 at 17 AR gene

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
TENM1	NM_001163278.2	c.7980C>T	p.Arg2660Arg	synonymous_variant	Exon 35 of 35		NP_001156750.1
TENM1	NM_001163279.1	c.7977C>T	p.Arg2659Arg	synonymous_variant	Exon 32 of 32		NP_001156751.1
TENM1	NM_014253.3	c.7959C>T	p.Arg2653Arg	synonymous_variant	Exon 31 of 31		NP_055068.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
TENM1	ENST00000371130.7	c.7959C>T	p.Arg2653Arg	synonymous_variant	Exon 31 of 31	1		ENSP00000360171.3
TENM1	ENST00000422452.3	c.7926C>T	p.Arg2642Arg	synonymous_variant	Exon 35 of 35	1		ENSP00000403954.4
STAG2	ENST00000469481.1	n.454-31067G>A		intron_variant	Intron 2 of 3	3

Frequencies

GnomAD3 genomes AF: 0.000716 AC: 80 AN: 111727 Hom.: 0 Cov.: 23 AF XY: 0.000501 AC XY: 17 AN XY: 33911

Gnomad AFR AF: 0.00225

Gnomad AMI AF: 0.00

Gnomad AMR AF: 0.000285

Gnomad ASJ AF: 0.00

Gnomad EAS AF: 0.00

Gnomad SAS AF: 0.00

Gnomad FIN AF: 0.00

Gnomad MID AF: 0.00

Gnomad NFE AF: 0.000151

Gnomad OTH AF: 0.00

GnomAD3 exomes AF: 0.000373 AC: 68 AN: 182469 Hom.: 0 AF XY: 0.000342 AC XY: 23 AN XY: 67173

Gnomad AFR exome AF: 0.00243

Gnomad AMR exome AF: 0.000840

Gnomad ASJ exome AF: 0.00

Gnomad EAS exome AF: 0.000217

Gnomad SAS exome AF: 0.00

Gnomad FIN exome AF: 0.00

Gnomad NFE exome AF: 0.000111

Gnomad OTH exome AF: 0.000222

GnomAD4 exome AF: 0.000151 AC: 166 AN: 1097615 Hom.: 0 Cov.: 30 AF XY: 0.000168 AC XY: 61 AN XY: 363025

Gnomad4 AFR exome AF: 0.00163

Gnomad4 AMR exome AF: 0.000767

Gnomad4 ASJ exome AF: 0.0000516

Gnomad4 EAS exome AF: 0.00

Gnomad4 SAS exome AF: 0.0000185

Gnomad4 FIN exome AF: 0.0000247

Gnomad4 NFE exome AF: 0.0000808

Gnomad4 OTH exome AF: 0.000456

GnomAD4 genome AF: 0.000716 AC: 80 AN: 111782 Hom.: 0 Cov.: 23 AF XY: 0.000500 AC XY: 17 AN XY: 33976

Gnomad4 AFR AF: 0.00224

Gnomad4 AMR AF: 0.000285

Gnomad4 ASJ AF: 0.00

Gnomad4 EAS AF: 0.00

Gnomad4 SAS AF: 0.00

Gnomad4 FIN AF: 0.00

Gnomad4 NFE AF: 0.000151

Gnomad4 OTH AF: 0.00

Alfa AF: 0.000564 Hom.: 1

Bravo AF: 0.00104

EpiCase AF: 0.000327

EpiControl AF: 0.000238

ClinVar

Significance: Benign

Submissions summary: Benign:2

Revision: criteria provided, single submitter

Submissions by phenotype

TENM1-related disorder Benign:1

Mar 25, 2019

PreventionGenetics, part of Exact Sciences

Significance: Likely benign

Review Status: no assertion criteria provided

Collection Method: clinical testing

This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications). -

not provided Benign:1

Oct 09, 2018

Labcorp Genetics (formerly Invitae), Labcorp

Significance: 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	-0.90
CADD	Benign	0.0090
DANN	Benign	0.79

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: rs139883667; hg19: chrX-123514605; COSMIC: COSV64431287;