NM_016138.5:c.73+1599T>G

Variant names:

• chr16-19069336-T-G
• rs7192898
• NM_016138.5:c.73+1599T>G

Variant summary

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

The NM_016138.5(COQ7):​c.73+1599T>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.556 in 151,514 control chromosomes in the GnomAD database, including 25,144 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 0.56 (25144 hom., cov: 30)
• Consequence: COQ7 NM_016138.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 1.12
• Publications: 1 publications found

Genes affected

COQ7 (HGNC:2244): (coenzyme Q7, hydroxylase) The protein encoded by this gene is similar to a mitochondrial di-iron containing hydroxylase in Saccharomyces cerevisiae that is involved with ubiquinone biosynthesis. Mutations in the yeast gene lead to slower development and longer life span. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jul 2010]

COQ7-DT (HGNC:55362): (COQ7 divergent transcript)

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.65).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.793 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_016138.5. 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
	COQ7	NM_016138.5	MANE Select	c.73+1599T>G		intron	N/A	NP_057222.2
	COQ7	NM_001370489.1		c.31+458T>G		intron	N/A	NP_001357418.1
	COQ7	NM_001370490.1		c.73+1599T>G		intron	N/A	NP_001357419.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	COQ7	ENST00000321998.10	TSL:1 MANE Select	c.73+1599T>G		intron	N/A	ENSP00000322316.5
	COQ7	ENST00000544894.6	TSL:1	c.-42+1328T>G		intron	N/A	ENSP00000442923.2
	COQ7	ENST00000568985.5	TSL:2	c.73+1599T>G		intron	N/A	ENSP00000456734.1

Frequencies

GnomAD3 genomes AF: 0.556 AC: 84197 AN: 151392 Hom.: 25124 Cov.: 30

Gnomad AFR AF: 0.328

Gnomad AMI AF: 0.615

Gnomad AMR AF: 0.614

Gnomad ASJ AF: 0.530

Gnomad EAS AF: 0.813

Gnomad SAS AF: 0.662

Gnomad FIN AF: 0.672

Gnomad MID AF: 0.580

Gnomad NFE AF: 0.636

Gnomad OTH AF: 0.613

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

GnomAD4 genome AF: 0.556 AC: 84258 AN: 151514 Hom.: 25144 Cov.: 30 AF XY: 0.564 AC XY: 41682 AN XY: 73928

African (AFR) AF: 0.328 AC: 13571 AN: 41352

American (AMR) AF: 0.614 AC: 9306 AN: 15146

Ashkenazi Jewish (ASJ) AF: 0.530 AC: 1839 AN: 3470

East Asian (EAS) AF: 0.813 AC: 4191 AN: 5154

South Asian (SAS) AF: 0.662 AC: 3183 AN: 4808

European-Finnish (FIN) AF: 0.672 AC: 6956 AN: 10352

Middle Eastern (MID) AF: 0.565 AC: 165 AN: 292

European-Non Finnish (NFE) AF: 0.636 AC: 43198 AN: 67928

Other (OTH) AF: 0.613 AC: 1292 AN: 2106

Alfa AF: 0.449 Hom.: 1761

Bravo AF: 0.545

Asia WGS AF: 0.742 AC: 2579 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.65
CADD	Benign	14
DANN	Benign	0.87
PhyloP100		1.1
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: rs7192898; hg19: chr16-19080658;