NM_001347969.2:c.-284-16516A>G

Variant names:

• chr13-43684060-T-C
• rs299352
• NM_001347969.2:c.-284-16516A>G

Variant summary

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

The NM_001347969.2(ENOX1):​c.-284-16516A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. 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 0.99 (72826 hom., cov: 20)
• Consequence: ENOX1 NM_001347969.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.00
• Publications: 1 publications found

Genes affected

ENOX1 (HGNC:25474): (ecto-NOX disulfide-thiol exchanger 1) The protein encoded by this gene is involved in plasma membrane electron transport pathways. The encoded protein has both a hydroquinone (NADH) oxidase activity and a protein disulfide-thiol interchange activity. The two activities cycle with a periodicity of 24 minutes, with one activity being at its peak when the other is at its lowest. [provided by RefSeq, Dec 2016]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.95).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.993 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
ENOX1	NM_001347969.2	c.-284-16516A>G		intron_variant	Intron 1 of 16	ENST00000690772.1	NP_001334898.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
ENOX1	ENST00000690772.1	c.-284-16516A>G		intron_variant	Intron 1 of 16		NM_001347969.2	ENSP00000509229.1
ENOX1	ENST00000261488.10	c.-321-16516A>G		intron_variant	Intron 1 of 16	1		ENSP00000261488.6

Frequencies

GnomAD3 genomes AF: 0.993 AC: 146548 AN: 147526 Hom.: 72793 Cov.: 20

Gnomad AFR AF: 0.980

Gnomad AMI AF: 1.00

Gnomad AMR AF: 0.997

Gnomad ASJ AF: 0.998

Gnomad EAS AF: 0.986

Gnomad SAS AF: 0.996

Gnomad FIN AF: 1.00

Gnomad MID AF: 0.997

Gnomad NFE AF: 1.00

Gnomad OTH AF: 0.994

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

GnomAD4 genome AF: 0.993 AC: 146626 AN: 147616 Hom.: 72826 Cov.: 20 AF XY: 0.993 AC XY: 71185 AN XY: 71678

African (AFR) AF: 0.979 AC: 38713 AN: 39524

American (AMR) AF: 0.997 AC: 14688 AN: 14728

Ashkenazi Jewish (ASJ) AF: 0.998 AC: 3458 AN: 3464

East Asian (EAS) AF: 0.986 AC: 4836 AN: 4906

South Asian (SAS) AF: 0.996 AC: 4555 AN: 4572

European-Finnish (FIN) AF: 1.00 AC: 9658 AN: 9658

Middle Eastern (MID) AF: 0.993 AC: 286 AN: 288

European-Non Finnish (NFE) AF: 1.00 AC: 67463 AN: 67494

Other (OTH) AF: 0.994 AC: 2061 AN: 2074

Alfa AF: 0.996 Hom.: 8103

Bravo AF: 0.992

Asia WGS AF: 0.987 AC: 3432 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.95
CADD	Benign	5.7
DANN	Benign	0.60
PhyloP100		0.0
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: rs299352; hg19: chr13-44258196;