rs1757106

Variant names:

• chr9-115083054-T-G
• rs1757106
• NM_002160.4:c.2132-247A>C

Your query was ambiguous. Multiple possible variants found:

• chr9-115083054-T-G
• chr9-115083054-T-A

Variant summary

Our verdict is Benign. The variant received -14 ACMG points: 0P and 14B. BP4_Strong BP6_Moderate BA1

The NM_002160.4(TNC):​c.2132-247A>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.564 in 152,054 control chromosomes in the GnomAD database, including 24,559 homozygotes. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Benign (★).

• Frequency: Genomes: 𝑓 0.56 (24559 hom., cov: 33)
• Consequence: TNC NM_002160.4 intron
• Clinical Significance: Benign criteria provided, single submitter B:1
• Conservation: PhyloP100: 1.89
• Publications: 2 publications found

Genes affected

TNC (HGNC:5318): (tenascin C) This gene encodes an extracellular matrix protein with a spatially and temporally restricted tissue distribution. This protein is homohexameric with disulfide-linked subunits, and contains multiple EGF-like and fibronectin type-III domains. It is implicated in guidance of migrating neurons as well as axons during development, synaptic plasticity, and neuronal regeneration. [provided by RefSeq, Jul 2011]

DELEC1 (HGNC:23658): (deleted in esophageal cancer 1) The function of this gene is not known. This gene is located in a region commonly deleted in esophageal squamous cell carcinomas. Gene expression is reduced or absent in these carcinomas and thus this is a candidate tumor suppressor gene for esophageal squamous cell carcinomas. [provided by RefSeq, Jul 2008]

ACMG classification

Our verdict: Benign. The variant received -14 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.78).
• BP6: Variant 9-115083054-T-G is Benign according to our data. Variant chr9-115083054-T-G is described in ClinVar as Benign. ClinVar VariationId is 1238384.Status of the report is criteria_provided_single_submitter, 1 stars.
• BA1: GnomAd4 highest subpopulation (AMR) allele frequency at 95% confidence interval = 0.634 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_002160.4. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	TNC	NM_002160.4	MANE Select	c.2132-247A>C		intron	N/A	NP_002151.2	P24821-1
	TNC	NM_001439065.1		c.2132-247A>C		intron	N/A	NP_001425994.1
	TNC	NM_001439066.1		c.2132-247A>C		intron	N/A	NP_001425995.1

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	TNC	ENST00000350763.9	TSL:1 MANE Select	c.2132-247A>C		intron	N/A	ENSP00000265131.4	P24821-1
	TNC	ENST00000423613.6	TSL:1	c.2132-247A>C		intron	N/A	ENSP00000411406.2	E9PC84
	TNC	ENST00000542877.6	TSL:1	c.2132-247A>C		intron	N/A	ENSP00000442242.1	F5H7V9

Frequencies

GnomAD3 genomes AF: 0.564 AC: 85649 AN: 151936 Hom.: 24520 Cov.: 33

Gnomad AFR AF: 0.621

Gnomad AMI AF: 0.423

Gnomad AMR AF: 0.645

Gnomad ASJ AF: 0.674

Gnomad EAS AF: 0.346

Gnomad SAS AF: 0.461

Gnomad FIN AF: 0.505

Gnomad MID AF: 0.665

Gnomad NFE AF: 0.538

Gnomad OTH AF: 0.589

We have no GnomAD4 exomes data on this position. Probably position not covered by the project.

GnomAD4 genome AF: 0.564 AC: 85748 AN: 152054 Hom.: 24559 Cov.: 33 AF XY: 0.562 AC XY: 41773 AN XY: 74338

African (AFR) AF: 0.622 AC: 25781 AN: 41454

American (AMR) AF: 0.645 AC: 9859 AN: 15282

Ashkenazi Jewish (ASJ) AF: 0.674 AC: 2340 AN: 3470

East Asian (EAS) AF: 0.346 AC: 1794 AN: 5182

South Asian (SAS) AF: 0.462 AC: 2224 AN: 4818

European-Finnish (FIN) AF: 0.505 AC: 5340 AN: 10564

Middle Eastern (MID) AF: 0.653 AC: 192 AN: 294

European-Non Finnish (NFE) AF: 0.538 AC: 36591 AN: 67972

Other (OTH) AF: 0.589 AC: 1241 AN: 2106

Alfa AF: 0.551 Hom.: 64284

Bravo AF: 0.577

Asia WGS AF: 0.479 AC: 1670 AN: 3478

ClinVar

ClinVar submissions

Significance: Benign

Revision: criteria provided, single submitter

Pathogenic	VUS	Benign	Condition
-	-	1	not provided (1)

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.78
CADD	Benign	12
DANN	Benign	0.66
PhyloP100		1.9
Mutation Taster		=100/0	polymorphism (auto)

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

Other links and lift over

dbSNP: rs1757106; hg19: chr9-117845333;