17-46751565-G-T

Variant names:

• chr17-46751565-G-T
• NM_006178.4:c.2106G>T

Variant summary

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

The NM_006178.4(NSF):​c.2106G>T​(p.Lys702Asn) 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. 14/21 in silico tools predict a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency: Genomes: not found (cov: 32)
• Consequence: NSF NM_006178.4 missense
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.551

Genes affected

NSF (HGNC:8016): (N-ethylmaleimide sensitive factor, vesicle fusing ATPase) Enables PDZ domain binding activity and ionotropic glutamate receptor binding activity. Involved in intracellular protein transport; positive regulation of protein catabolic process; and positive regulation of receptor recycling. Located in Golgi apparatus; cytosol; and plasma membrane. Implicated in developmental and epileptic encephalopathy. [provided by Alliance of Genome Resources, Apr 2022]

LRRC37A2 (HGNC:32404): (leucine rich repeat containing 37 member A2) Predicted to be integral component of membrane. [provided by Alliance of Genome Resources, Apr 2022]

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=0.2722503).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
NSF	NM_006178.4	c.2106G>T	p.Lys702Asn	missense_variant	Exon 19 of 21	ENST00000398238.8	NP_006169.2
LRRC37A2	XM_024450773.2	c.4809+201046G>T		intron_variant	Intron 10 of 10		XP_024306541.1
NSF	NR_040116.2	n.2173G>T		non_coding_transcript_exon_variant	Exon 18 of 20

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
NSF	ENST00000398238.8	c.2106G>T	p.Lys702Asn	missense_variant	Exon 19 of 21	1	NM_006178.4	ENSP00000381293.4

Frequencies

GnomAD3 genomes Cov.: 32

GnomAD4 exome Cov.: 31

GnomAD4 genome Cov.: 32

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.17
BayesDel_addAF	Benign	-0.097	T
BayesDel_noAF	Benign	-0.38
CADD	Benign	16
DANN	Uncertain	0.99
DEOGEN2	Benign	0.12	T;T;T
Eigen	Benign	-0.72
Eigen_PC	Benign	-0.57
FATHMM_MKL	Benign	0.37	N
M_CAP	Benign	0.032	D
MetaRNN	Benign	0.27	T;T;T
MetaSVM	Benign	-0.44	T
MutationAssessor	Benign	0.0	N;.;.
PrimateAI	Uncertain	0.60	T
PROVEAN	Benign	-1.1	N;.;.
REVEL	Benign	0.28
Sift	Benign	0.16	T;.;.
Sift4G	Benign	0.21	T;T;T
Polyphen		0.0	B;.;.
Vest4		0.096
MutPred		0.53		Loss of methylation at K702 (P = 0.005);.;.;
MVP		0.42
MPC		0.64
ClinPred		0.17	T
GERP RS		0.64
Varity_R		0.064
gMVP		0.37

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: chr17-44828931;