chr9-69328086-C-T

Variant names:

• chr9-69328086-C-T
• rs3750552
• NM_001347995.2:c.414+2363C>T

Variant summary

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

The NM_001347995.2(ENTREP1):​c.414+2363C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.711 in 151,976 control chromosomes in the GnomAD database, including 38,897 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 0.71 (38897 hom., cov: 31)
• Consequence: ENTREP1 NM_001347995.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.703
• Publications: 9 publications found

Genes affected

ENTREP1 (HGNC:24820): (endosomal transmembrane epsin interactor 1) Predicted to be integral component of membrane. [provided by Alliance of Genome Resources, Apr 2022]

ENTREP1 Gene-Disease associations (from GenCC):

• schizophrenia

  Inheritance: Unknown Classification: NO_KNOWN Submitted by: Labcorp Genetics (formerly Invitae)

ACMG classification

Our verdict: Benign. The variant received -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.94).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.778 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001347995.2. 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
	ENTREP1	NM_001347995.2	MANE Select	c.414+2363C>T		intron	N/A	NP_001334924.1
	ENTREP1	NM_001127608.3		c.-46+3456C>T		intron	N/A	NP_001121080.1
	ENTREP1	NR_170669.1		n.50+3456C>T		intron	N/A

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	ENTREP1	ENST00000303068.14	TSL:2 MANE Select	c.414+2363C>T		intron	N/A	ENSP00000304435.8
	ENTREP1	ENST00000377216.4	TSL:1	n.-46+3456C>T		intron	N/A	ENSP00000366422.4
	ENTREP1	ENST00000455972.6	TSL:5	c.-46+3456C>T		intron	N/A	ENSP00000395675.1

Frequencies

GnomAD3 genomes AF: 0.711 AC: 108042 AN: 151858 Hom.: 38883 Cov.: 31

Gnomad AFR AF: 0.603

Gnomad AMI AF: 0.876

Gnomad AMR AF: 0.733

Gnomad ASJ AF: 0.651

Gnomad EAS AF: 0.696

Gnomad SAS AF: 0.799

Gnomad FIN AF: 0.810

Gnomad MID AF: 0.661

Gnomad NFE AF: 0.753

Gnomad OTH AF: 0.705

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

GnomAD4 genome AF: 0.711 AC: 108099 AN: 151976 Hom.: 38897 Cov.: 31 AF XY: 0.714 AC XY: 53077 AN XY: 74292

African (AFR) AF: 0.602 AC: 24940 AN: 41400

American (AMR) AF: 0.734 AC: 11191 AN: 15256

Ashkenazi Jewish (ASJ) AF: 0.651 AC: 2255 AN: 3466

East Asian (EAS) AF: 0.697 AC: 3592 AN: 5156

South Asian (SAS) AF: 0.799 AC: 3845 AN: 4810

European-Finnish (FIN) AF: 0.810 AC: 8575 AN: 10584

Middle Eastern (MID) AF: 0.667 AC: 196 AN: 294

European-Non Finnish (NFE) AF: 0.753 AC: 51215 AN: 67994

Other (OTH) AF: 0.709 AC: 1491 AN: 2104

Alfa AF: 0.728 Hom.: 60348

Bravo AF: 0.694

Asia WGS AF: 0.747 AC: 2598 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.94
CADD	Benign	1.4
DANN	Benign	0.63
PhyloP100		-0.70
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: rs3750552; hg19: chr9-71943002;