rs10408676

chr19-15179196-C-Achr19-15179196-C-Gchr19-15179196-C-T

Variant summary

Our verdict is Uncertain significance. Variant got 3 ACMG points: 3P and 0B. PM2 PP3

The NM_000435.3(NOTCH3):c.3547G>T(p.Val1183Leu) 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 pathogenic outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar. Another variant affecting the same amino acid position, but resulting in a different missense (i.e. V1183M) has been classified as Benign.

• Frequency: Genomes: not found (cov: 34)
• Consequence: NOTCH3 NM_000435.3 missense
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 2.97

Genes affected

NOTCH3 (HGNC:7883): (notch receptor 3) This gene encodes the third discovered human homologue of the Drosophilia melanogaster type I membrane protein notch. In Drosophilia, notch interaction with its cell-bound ligands (delta, serrate) establishes an intercellular signalling pathway that plays a key role in neural development. Homologues of the notch-ligands have also been identified in human, but precise interactions between these ligands and the human notch homologues remains to be determined. Mutations in NOTCH3 have been identified as the underlying cause of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). [provided by RefSeq, Jul 2008]

ACMG classification

Verdict is Uncertain_significance. Variant got 3 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• PP3: MetaRNN computational evidence supports a deleterious effect, 0.785

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
NOTCH3	NM_000435.3	c.3547G>T	p.Val1183Leu	missense_variant	22/33	ENST00000263388.7
NOTCH3	XM_005259924.5	c.3391G>T	p.Val1131Leu	missense_variant	21/32

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
NOTCH3	ENST00000263388.7	c.3547G>T	p.Val1183Leu	missense_variant	22/33	1	NM_000435.3	P1
NOTCH3	ENST00000601011.1	c.3388G>T	p.Val1130Leu	missense_variant	21/23	5
NOTCH3	ENST00000595045.1	n.383G>T		non_coding_transcript_exon_variant	2/3	2
NOTCH3	ENST00000600841.1	n.25G>T		non_coding_transcript_exon_variant	1/2	2

Frequencies

GnomAD3 genomes Cov.: 34

GnomAD4 exome Cov.: 36

GnomAD4 genome Cov.: 34

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.14
BayesDel_addAF	Uncertain	0.13	D
BayesDel_noAF	Uncertain	-0.050
Cadd	Benign	21
Dann	Uncertain	1.0
DEOGEN2	Uncertain	0.54	D;T
Eigen	Benign	-0.050
Eigen_PC	Benign	0.032
FATHMM_MKL	Pathogenic	0.97	D
LIST_S2	Benign	0.77	T;T
M_CAP	Uncertain	0.27	D
MetaRNN	Pathogenic	0.78	D;D
MetaSVM	Uncertain	0.64	D
MutationAssessor	Benign	1.5	L;.
MutationTaster	Benign	0.00037	P
PrimateAI	Uncertain	0.57	T
PROVEAN	Benign	-2.3	N;.
REVEL	Uncertain	0.51
Sift	Benign	0.12	T;.
Sift4G	Benign	0.16	T;T
Polyphen		0.063	B;.
Vest4		0.52
MutPred		0.55		Gain of disorder (P = 0.1228);.;
MVP		0.85
MPC		0.70
ClinPred		0.68	D
GERP RS		3.9
Varity_R		0.27
gMVP		0.49

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

No publications associated with this variant yet.

Other links and lift over

hg19: chr19-15290007;