rs1554398288

Positions:

• chr7-116771580-T-A
• chr7-116771580-T-C
• chr7-116771580-T-G

Variant summary

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

The NM_000245.4(MET):​c.2813T>A​(p.Val938Asp) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. 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. V938A) has been classified as Uncertain significance.

• Frequency: Genomes: not found (cov: 32)
• Consequence: MET NM_000245.4 missense
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 1.60

Genes affected

MET (HGNC:7029): (MET proto-oncogene, receptor tyrosine kinase) This gene encodes a member of the receptor tyrosine kinase family of proteins and the product of the proto-oncogene MET. The encoded preproprotein is proteolytically processed to generate alpha and beta subunits that are linked via disulfide bonds to form the mature receptor. Further processing of the beta subunit results in the formation of the M10 peptide, which has been shown to reduce lung fibrosis. Binding of its ligand, hepatocyte growth factor, induces dimerization and activation of the receptor, which plays a role in cellular survival, embryogenesis, and cellular migration and invasion. Mutations in this gene are associated with papillary renal cell carcinoma, hepatocellular carcinoma, and various head and neck cancers. Amplification and overexpression of this gene are also associated with multiple human cancers. [provided by RefSeq, May 2016]

ACMG classification

Verdict is Uncertain_significance. Variant got 2 ACMG points.

• PM2: Very rare variant in population databases, with high coverage

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
MET	NM_000245.4	c.2813T>A	p.Val938Asp	missense_variant	13/21	ENST00000397752.8
MET	NM_001127500.3	c.2867T>A	p.Val956Asp	missense_variant	13/21
MET	NM_001324402.2	c.1523T>A	p.Val508Asp	missense_variant	12/20
MET	XM_011516223.2	c.2870T>A	p.Val957Asp	missense_variant	14/22

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
MET	ENST00000397752.8	c.2813T>A	p.Val938Asp	missense_variant	13/21	1	NM_000245.4	P3
MET	ENST00000318493.11	c.2867T>A	p.Val956Asp	missense_variant	13/21	1		A2
MET	ENST00000436117.3	c.*418T>A		3_prime_UTR_variant, NMD_transcript_variant	12/20	1
MET	ENST00000454623.1	c.209T>A	p.Val70Asp	missense_variant	2/3	5

Frequencies

GnomAD3 genomes Cov.: 32

GnomAD4 exome Cov.: 32

GnomAD4 genome Cov.: 32

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Pathogenic	0.74
BayesDel_addAF	Pathogenic	0.25	D
BayesDel_noAF	Uncertain	0.12
CADD	Benign	21
DANN	Benign	0.97
DEOGEN2	Pathogenic	0.89	D;.;.
Eigen	Benign	-0.14
Eigen_PC	Benign	-0.12
FATHMM_MKL	Uncertain	0.76	D
LIST_S2	Uncertain	0.94	D;D;D
M_CAP	Uncertain	0.10	D
MetaRNN	Uncertain	0.59	D;D;D
MetaSVM	Benign	-0.62	T
MutationAssessor	Benign	1.6	L;.;.
MutationTaster	Benign	1.0	D;D
PrimateAI	Benign	0.38	T
PROVEAN	Uncertain	-4.2	D;D;D
REVEL	Uncertain	0.48
Sift	Uncertain	0.0080	D;D;D
Sift4G	Uncertain	0.0070	D;D;D
Polyphen		0.50	P;B;.
Vest4		0.47
MutPred		0.48		Gain of sheet (P = 0.0149);.;.;
MVP		0.99
MPC		0.78
ClinPred		0.98	D
GERP RS		0.41
Varity_R		0.44
gMVP		0.81

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.060		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: chr7-116411634;