9-115016064-C-T

Variant names:

• chr9-115016064-C-T
• rs12156617
• ENST00000648852.1:n.276+46403C>T

Variant summary

Our verdict is Benign. The variant received -12 ACMG points: 0P and 12B. BP4_Strong BA1

The ENST00000648852.1(DELEC1):​n.276+46403C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.127 in 152,202 control chromosomes in the GnomAD database, including 2,244 homozygotes. In-silico tool predicts a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency: Genomes: 𝑓 0.13 (2244 hom., cov: 32)
• Consequence: DELEC1 ENST00000648852.1 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.0140
• Publications: 2 publications found

Genes affected

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 -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.87).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.307 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000648852.1. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
There are no transcript annotations for this variant.

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	DELEC1	ENST00000648852.1		n.276+46403C>T		intron	N/A
	DELEC1	ENST00000649121.1		n.78+46403C>T		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.127 AC: 19344 AN: 152086 Hom.: 2239 Cov.: 32

Gnomad AFR AF: 0.312

Gnomad AMI AF: 0.0954

Gnomad AMR AF: 0.0808

Gnomad ASJ AF: 0.0878

Gnomad EAS AF: 0.0241

Gnomad SAS AF: 0.0607

Gnomad FIN AF: 0.0214

Gnomad MID AF: 0.194

Gnomad NFE AF: 0.0569

Gnomad OTH AF: 0.111

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

GnomAD4 genome AF: 0.127 AC: 19371 AN: 152202 Hom.: 2244 Cov.: 32 AF XY: 0.123 AC XY: 9141 AN XY: 74408

African (AFR) AF: 0.312 AC: 12940 AN: 41486

American (AMR) AF: 0.0807 AC: 1235 AN: 15296

Ashkenazi Jewish (ASJ) AF: 0.0878 AC: 305 AN: 3472

East Asian (EAS) AF: 0.0244 AC: 126 AN: 5174

South Asian (SAS) AF: 0.0603 AC: 291 AN: 4822

European-Finnish (FIN) AF: 0.0214 AC: 227 AN: 10620

Middle Eastern (MID) AF: 0.199 AC: 58 AN: 292

European-Non Finnish (NFE) AF: 0.0569 AC: 3870 AN: 68016

Other (OTH) AF: 0.110 AC: 232 AN: 2112

Alfa AF: 0.103 Hom.: 189

Bravo AF: 0.140

Asia WGS AF: 0.0470 AC: 165 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.87
CADD	Benign	6.1
DANN	Benign	0.82
PhyloP100		-0.014

Splicing

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Other links and lift over

dbSNP: rs12156617; hg19: chr9-117778343;