rs10435378

chr7-116785439-G-Achr7-116785439-G-T

Variant summary

Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_000245.4(MET):c.3798+1970G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.648 in 152,012 control chromosomes in the GnomAD database, including 33,728 homozygotes. In-silico tool predicts a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency: Genomes: 𝑓 0.65 (33728 hom., cov: 31)
• Consequence: MET NM_000245.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.924

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 Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.9).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.888 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
MET	NM_000245.4	c.3798+1970G>A		intron_variant		ENST00000397752.8
MET	NM_001127500.3	c.3852+1970G>A		intron_variant
MET	NM_001324402.2	c.2508+1970G>A		intron_variant
MET	XM_011516223.2	c.3855+1970G>A		intron_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
MET	ENST00000397752.8	c.3798+1970G>A		intron_variant		1	NM_000245.4	P3
MET	ENST00000318493.11	c.3852+1970G>A		intron_variant		1		A2
MET	ENST00000436117.3	c.*1403+1970G>A		intron_variant, NMD_transcript_variant		1

Frequencies

GnomAD3 genomes AF: 0.648 AC: 98376 AN: 151894 Hom.: 33655 Cov.: 31

Gnomad AFR AF: 0.895

Gnomad AMI AF: 0.693

Gnomad AMR AF: 0.553

Gnomad ASJ AF: 0.513

Gnomad EAS AF: 0.522

Gnomad SAS AF: 0.538

Gnomad FIN AF: 0.618

Gnomad MID AF: 0.570

Gnomad NFE AF: 0.548

Gnomad OTH AF: 0.606

We have no GnomAD4 exomes data on this position. Probably position not covered by the project.

GnomAD4 genome AF: 0.648 AC: 98522 AN: 152012 Hom.: 33728 Cov.: 31 AF XY: 0.645 AC XY: 47951 AN XY: 74288

Gnomad4 AFR AF: 0.896

Gnomad4 AMR AF: 0.553

Gnomad4 ASJ AF: 0.513

Gnomad4 EAS AF: 0.522

Gnomad4 SAS AF: 0.540

Gnomad4 FIN AF: 0.618

Gnomad4 NFE AF: 0.548

Gnomad4 OTH AF: 0.611

Alfa AF: 0.618 Hom.: 4431

Bravo AF: 0.653

Asia WGS AF: 0.575 AC: 2000 AN: 3476

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.90
Cadd	Benign	0.78
Dann	Benign	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

LitVar

Other links and lift over

dbSNP: rs10435378; hg19: chr7-116425493;