8-42395122-T-G

Position:

• chr8-42395122-T-G

Variant summary

Our verdict is Uncertain significance. Variant got 0 ACMG points: 2P and 2B. PM2 BP4_Moderate

The NM_005662.7(VDAC3):​c.106T>G​(p.Cys36Gly) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. In-silico tool predicts a benign outcome for this variant. 15/21 in silico tools predict a benign outcome for this variant. Variant has been reported in ClinVar as Uncertain significance (★).

• Frequency: Genomes: not found (cov: 32)
• Consequence: VDAC3 NM_005662.7 missense
• Clinical Significance: Uncertain significance criteria provided, single submitter U:1
• Conservation: PhyloP100: 0.754

Genes affected

VDAC3 (HGNC:12674): (voltage dependent anion channel 3) This gene encodes a voltage-dependent anion channel (VDAC), and belongs to the mitochondrial porin family. VDACs are small, integral membrane proteins that traverse the outer mitochondrial membrane and conduct ATP and other small metabolites. They are known to bind several kinases of intermediary metabolism, thought to be involved in translocation of adenine nucleotides, and are hypothesized to form part of the mitochondrial permeability transition pore, which results in the release of cytochrome c at the onset of apoptotic cell death. Alternatively transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Oct 2011]

ACMG classification

Verdict is Uncertain_significance. Variant got 0 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (MetaRNN=0.12432933).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
VDAC3	NM_005662.7	c.106T>G	p.Cys36Gly	missense_variant	4/10	ENST00000022615.9	NP_005653.3

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
VDAC3	ENST00000022615.9	c.106T>G	p.Cys36Gly	missense_variant	4/10	1	NM_005662.7	ENSP00000022615	P4

Frequencies

GnomAD3 genomes Cov.: 32

GnomAD4 exome Cov.: 31

GnomAD4 genome Cov.: 32

ClinVar

Significance: Uncertain significance

Submissions summary: Uncertain:1

Revision: criteria provided, single submitter

Submissions by phenotype

not specified Uncertain:1

Uncertain significance, criteria provided, single submitter

clinical testing

Ambry Genetics

Dec 13, 2022

The c.106T>G (p.C36G) alteration is located in exon 4 (coding exon 2) of the VDAC3 gene. This alteration results from a T to G substitution at nucleotide position 106, causing the cysteine (C) at amino acid position 36 to be replaced by a glycine (G). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear. -

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.069
BayesDel_addAF	Benign	-0.15	T
BayesDel_noAF	Benign	-0.46
CADD	Benign	22
DANN	Benign	0.86
DEOGEN2	Benign	0.10	.;.;.;.;T
Eigen	Benign	-0.28
Eigen_PC	Benign	-0.056
FATHMM_MKL	Uncertain	0.83	D
LIST_S2	Benign	0.80	T;T;T;T;T
M_CAP	Benign	0.0075	T
MetaRNN	Benign	0.12	T;T;T;T;T
MetaSVM	Benign	-1.0	T
MutationAssessor	Benign	0.69	.;.;.;N;N
MutationTaster	Benign	0.60	N;N;N;N
PrimateAI	Benign	0.45	T
PROVEAN	Benign	-0.62	N;N;N;N;N
REVEL	Benign	0.083
Sift	Benign	0.40	T;T;T;T;T
Sift4G	Benign	0.33	T;T;T;T;T
Polyphen		0.011	.;.;.;.;B
Vest4		0.46, 0.40, 0.36
MutPred		0.39		Gain of disorder (P = 0.0117);Gain of disorder (P = 0.0117);Gain of disorder (P = 0.0117);Gain of disorder (P = 0.0117);Gain of disorder (P = 0.0117);
MVP		0.043
MPC		0.25
ClinPred		0.32	T
GERP RS		5.5
Varity_R		0.19
gMVP		0.090

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

Publications

No publications associated with this variant yet.

Other links and lift over

hg19: chr8-42252640;