7-81758726-T-A

Position:

• chr7-81758726-T-A

Variant summary

Our verdict is Likely benign. Variant got -2 ACMG points: 2P and 4B. PM2 BP4_Strong

The NM_000601.6(HGF):​c.333A>T​(p.Glu111Asp) 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. 16/21 in silico tools predict a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar. Synonymous variant affecting the same amino acid position (i.e. E111E) has been classified as Likely benign.

• Frequency: Genomes: not found (cov: 32)
• Consequence: HGF NM_000601.6 missense
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.990

Genes affected

HGF (HGNC:4893): (hepatocyte growth factor) This gene encodes a protein that binds to the hepatocyte growth factor receptor to regulate cell growth, cell motility and morphogenesis in numerous cell and tissue types. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed to generate alpha and beta chains, which form the mature heterodimer. This protein is secreted by mesenchymal cells and acts as a multi-functional cytokine on cells of mainly epithelial origin. This protein also plays a role in angiogenesis, tumorogenesis, and tissue regeneration. Although the encoded protein is a member of the peptidase S1 family of serine proteases, it lacks peptidase activity. Mutations in this gene are associated with nonsyndromic hearing loss. [provided by RefSeq, Nov 2015]

ACMG classification

Verdict is Likely_benign. Variant got -2 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (MetaRNN=0.055708557).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
HGF	NM_000601.6	c.333A>T	p.Glu111Asp	missense_variant	3/18	ENST00000222390.11

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
HGF	ENST00000222390.11	c.333A>T	p.Glu111Asp	missense_variant	3/18	1	NM_000601.6	P4

Frequencies

GnomAD3 genomes Cov.: 32

GnomAD4 exome Cov.: 29

GnomAD4 genome Cov.: 32

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.12
BayesDel_addAF	Benign	-0.15	T
BayesDel_noAF	Benign	-0.45
CADD	Benign	0.47
DANN	Benign	0.97
DEOGEN2	Uncertain	0.66	D;D;.;.;.;.;.;D;D;.;T
Eigen	Benign	-1.6
Eigen_PC	Benign	-1.6
FATHMM_MKL	Benign	0.11	N
LIST_S2	Benign	0.71	.;T;T;T;T;T;T;T;T;T;T
M_CAP	Benign	0.078	D
MetaRNN	Benign	0.056	T;T;T;T;T;T;T;T;T;T;T
MetaSVM	Benign	-0.74	T
MutationAssessor	Benign	1.0	L;L;L;L;L;L;.;.;.;.;.
MutationTaster	Benign	1.0	P;P;P;P;P;P;P
PrimateAI	Benign	0.27	T
PROVEAN	Benign	-1.4	.;N;N;N;N;N;.;N;.;N;N
REVEL	Benign	0.20
Sift	Benign	0.079	.;T;T;T;T;T;.;T;.;T;T
Sift4G	Benign	0.11	.;T;D;T;T;T;.;T;.;.;.
Polyphen		0.0	B;B;B;B;B;.;.;.;.;.;.
Vest4		0.084, 0.081, 0.092, 0.076, 0.091
MutPred		0.40		Loss of methylation at K109 (P = 0.1021);Loss of methylation at K109 (P = 0.1021);Loss of methylation at K109 (P = 0.1021);Loss of methylation at K109 (P = 0.1021);Loss of methylation at K109 (P = 0.1021);Loss of methylation at K109 (P = 0.1021);Loss of methylation at K109 (P = 0.1021);Loss of methylation at K109 (P = 0.1021);Loss of methylation at K109 (P = 0.1021);Loss of methylation at K109 (P = 0.1021);Loss of methylation at K109 (P = 0.1021);
MVP		0.53
MPC		0.45
ClinPred		0.19	T
GERP RS		-3.0
Varity_R		0.34
gMVP		0.55

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: chr7-81388042;