22-40779109-C-A

Variant names:

• chr22-40779109-C-A
• rs2057272986
• NM_006358.4:c.351G>T

Variant summary

Our verdict is Uncertain significance. Variant got 1 ACMG points: 2P and 1B. PM2 BP4

The NM_006358.4(SLC25A17):​c.351G>T​(p.Leu117Phe) 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. Variant has been reported in ClinVar as Uncertain significance (★).

• Frequency: Genomes: not found (cov: 32)
• Consequence: SLC25A17 NM_006358.4 missense
• Clinical Significance: Uncertain significance criteria provided, single submitter U:1
• Conservation: PhyloP100: 0.347

Genes affected

SLC25A17 (HGNC:10987): (solute carrier family 25 member 17) This gene encodes a peroxisomal membrane protein that belongs to the family of mitochondrial solute carriers. It is expressed in the liver, and is likely involved in transport. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]

ACMG classification

Verdict is Uncertain_significance. Variant got 1 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (MetaRNN=0.4192189).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
SLC25A17	NM_006358.4	c.351G>T	p.Leu117Phe	missense_variant	Exon 5 of 9	ENST00000435456.7	NP_006349.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
SLC25A17	ENST00000435456.7	c.351G>T	p.Leu117Phe	missense_variant	Exon 5 of 9	1	NM_006358.4	ENSP00000390722.2

Frequencies

GnomAD3 genomes Cov.: 32

GnomAD4 exome Cov.: 30

GnomAD4 genome Cov.: 32

Alfa AF: 0.0000936 Hom.: 0

Bravo AF: 0.00000756

ClinVar

Significance: Uncertain significance

Submissions summary: Uncertain:1

Revision: criteria provided, single submitter

Submissions by phenotype

not specified Uncertain:1

Feb 08, 2025

Ambry Genetics

Significance: Uncertain significance

Review Status: criteria provided, single submitter

Collection Method: clinical testing

The c.351G>T (p.L117F) alteration is located in exon 5 (coding exon 5) of the SLC25A17 gene. This alteration results from a G to T substitution at nucleotide position 351, causing the leucine (L) at amino acid position 117 to be replaced by a phenylalanine (F). 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	0.16
BayesDel_addAF	Uncertain	0.034	T
BayesDel_noAF	Benign	-0.19
CADD	Benign	22
DANN	Uncertain	1.0
DEOGEN2	Benign	0.31	T;.;T
Eigen	Benign	0.084
Eigen_PC	Uncertain	0.24
FATHMM_MKL	Uncertain	0.86	D
LIST_S2	Uncertain	0.93	D;D;D
M_CAP	Benign	0.040	D
MetaRNN	Benign	0.42	T;T;T
MetaSVM	Benign	-0.38	T
MutationAssessor	Benign	1.0	L;.;.
PrimateAI	Pathogenic	0.91	D
PROVEAN	Uncertain	-2.7	D;.;N
REVEL	Uncertain	0.41
Sift	Benign	0.14	T;.;T
Sift4G	Benign	0.24	T;T;T
Polyphen		0.21	B;.;.
Vest4		0.54
MutPred		0.65		Gain of catalytic residue at L117 (P = 0.0966);.;.;
MVP		0.82
MPC		0.72
ClinPred		0.92	D
GERP RS		5.0
Varity_R		0.34
gMVP		0.76

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.010		Details are displayed if max score is > 0.2

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

Publications

LitVar

Other links and lift over

dbSNP: rs2057272986; hg19: chr22-41175113;