NDUFAF6 p.Gln99Arg

Variant names:

• chr8-95032093-A-G
• rs137853184
• NM_152416.4:c.296A>G
• NDUFAF6 p.Gln99Arg

Your query was ambiguous. Multiple possible variants found:

• chr8-95032093-A-G
• chr8-95032093-AG-GT
• chr8-95032093-AG-GC
• chr8-95032093-AG-GA
• chr8-95032092-CAG-AGA
• chr8-95032092-CA-AG

Variant summary

Our verdict is Uncertain significance. The variant received 5 ACMG points: 5P and 0B. PM2 PP3_Moderate PP5

The NM_152416.4(NDUFAF6):​c.296A>G​(p.Gln99Arg) variant causes a missense, splice region change involving the alteration of a conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. In-silico tool predicts a pathogenic outcome for this variant. Variant has been reported in ClinVar as Pathogenic (no stars).

• Frequency: Genomes: not found (cov: 33)
• Consequence: NDUFAF6 NM_152416.4 missense, splice_region
• Clinical Significance: Pathogenic no assertion criteria provided P:1
• Conservation: PhyloP100: 8.78
• Publications: 9 publications found

Genes affected

NDUFAF6 (HGNC:28625): (NADH:ubiquinone oxidoreductase complex assembly factor 6) This gene encodes a protein that localizes to mitochondria and contains a predicted phytoene synthase domain. The encoded protein plays an important role in the assembly of complex I (NADH-ubiquinone oxidoreductase) of the mitochondrial respiratory chain through regulation of subunit ND1 biogenesis. Mutations in this gene are associated with complex I enzymatic deficiency. [provided by RefSeq, Nov 2011]

NDUFAF6 Gene-Disease associations (from GenCC):

• Leigh syndrome

  Inheritance: AR Classification: DEFINITIVE Submitted by: ClinGen
• mitochondrial disease

  Inheritance: AR Classification: DEFINITIVE Submitted by: ClinGen
• mitochondrial complex I deficiency, nuclear type 17

  Inheritance: AR Classification: MODERATE Submitted by: Ambry Genetics
• primary Fanconi syndrome

  Inheritance: AD Classification: SUPPORTIVE Submitted by: Orphanet
• Leigh syndrome with leukodystrophy

  Inheritance: AR Classification: SUPPORTIVE Submitted by: Orphanet
• Fanconi renotubular syndrome 5

  Inheritance: AR Classification: LIMITED Submitted by: Ambry Genetics

ACMG classification

Our verdict: Uncertain_significance. The variant received 5 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• PP3: MetaRNN computational evidence supports a deleterious effect, 0.878
• PP5: Variant 8-95032093-A-G is Pathogenic according to our data. Variant chr8-95032093-A-G is described in ClinVar as Pathogenic. ClinVar VariationId is 547.Status of the report is no_assertion_criteria_provided, 0 stars.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_152416.4. 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
	NDUFAF6	NM_152416.4	MANE Select	c.296A>G	p.Gln99Arg	missense splice_region	Exon 2 of 9	NP_689629.2	Q330K2-1
	NDUFAF6	NM_001330582.2		c.16A>G	p.Arg6Gly	missense	Exon 2 of 9	NP_001317511.1	A0A075B6P0
	NDUFAF6	NM_001354514.2		c.16A>G	p.Arg6Gly	missense	Exon 5 of 12	NP_001341443.1	A0A075B6P0

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	NDUFAF6	ENST00000396124.9	TSL:2 MANE Select	c.296A>G	p.Gln99Arg	missense splice_region	Exon 2 of 9	ENSP00000379430.4	Q330K2-1
	NDUFAF6	ENST00000396111.6	TSL:5	c.16A>G	p.Arg6Gly	missense	Exon 3 of 10	ENSP00000379417.1	A0A075B6P0
	NDUFAF6	ENST00000396113.5	TSL:5	c.16A>G	p.Arg6Gly	missense	Exon 8 of 15	ENSP00000379419.1	A0A075B6P0

Frequencies

GnomAD3 genomes Cov.: 33

GnomAD4 exome Cov.: 30

GnomAD4 genome Cov.: 33

ClinVar

ClinVar submissions

Significance: Pathogenic

Revision: no assertion criteria provided

Pathogenic	VUS	Benign	Condition
1	-	-	Mitochondrial complex I deficiency, nuclear type 17 (1)

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.18
BayesDel_addAF	Pathogenic	0.31	D
BayesDel_noAF	Pathogenic	0.21
CADD	Uncertain	25
DANN	Benign	0.81
DEOGEN2	Benign	0.19	T
Eigen	Uncertain	0.44
Eigen_PC	Uncertain	0.48
FATHMM_MKL	Pathogenic	0.98	D
LIST_S2	Benign	0.70	T
M_CAP	Benign	0.071	D
MetaRNN	Pathogenic	0.88	D
MetaSVM	Benign	-0.36	T
MutationAssessor	Benign	0.085	N
PhyloP100		8.8
PrimateAI	Uncertain	0.56	T
PROVEAN	Benign	-0.77	N
REVEL	Uncertain	0.39
Sift	Benign	0.36	T
Sift4G	Benign	0.99	T
Varity_R		0.15
gMVP		0.51
Mutation Taster		=114/186	disease causing (ClinVar)

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.26		Details are displayed if max score is > 0.2
DS_DL_spliceai		0.26		Position offset: 1

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

MaxEntScan Visualizer can be used to analyze the impact of this mutation on the neighboring sequence.

Other links and lift over

dbSNP: rs137853184;

hg19: chr8-96044321;