12-6019277-T-C

Position:

chr12-6019277-T-C

Variant summary

Our verdict is Benign. Variant got -10 ACMG points: 0P and 10B. BP4BA1BP5

This summary comes from the ClinGen Evidence Repository: The missense variant NM_000552.5(VWF):c.4141A>G (p.Thr1381Ala) is common in the general population with a Grpmax filtering allele frequency of 0.8925 (based on 67313/74942 alleles in the African/African American population) in gnomAD v4.1 (BA1). Several probands have been reported (PMID:30817071, PMID:30762591) with Thr1381Ala in cis or trans with additional vWF variants, including the type 2B Arg1308Cys variant (ClinVar 289, classified Pathogenic by the ClinGen VWD VCEP; BP5). and therefore meets criteria to be classified as benign for von Willebrand disease based on the ACMG/AMP criteria applied, as specified by the ClinGen VWD: BA1, BP4, BP5 (VCEP Rule specifications for von Willebrand disease type 2A, 2B and 2M v1.0.0; 08/12/2024). LINK:https://erepo.genome.network/evrepo/ui/classification/CA6402593/MONDO:0019565/090

Frequency

Genomes: 𝑓 0.72 ( 39998 hom., cov: 30)

Exomes 𝑓: 0.64 ( 301018 hom. )

Consequence

VWF
NM_000552.5 missense

Scores

Clinical Significance

Benign reviewed by expert panel U:1B:11

Conservation

PhyloP100: 1.88

Variant links:

Genes affected

VWF (HGNC:12726): (von Willebrand factor) This gene encodes a glycoprotein involved in hemostasis. The encoded preproprotein is proteolytically processed following assembly into large multimeric complexes. These complexes function in the adhesion of platelets to sites of vascular injury and the transport of various proteins in the blood. Mutations in this gene result in von Willebrand disease, an inherited bleeding disorder. An unprocessed pseudogene has been found on chromosome 22. [provided by RefSeq, Oct 2015]

VWF links:

VWF (HGNC:):

VWF links:

Genome browser will be placed here

ACMG classification

Classification made for transcript

Verdict is Benign. Variant got -10 ACMG points.

BP4

For more information check the summary or visit ClinGen Evidence Repository.

BP5

For more information check the summary or visit ClinGen Evidence Repository.

BA1

For more information check the summary or visit ClinGen Evidence Repository.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
VWF	NM_000552.5 linkuse as main transcript	c.4141A>G	p.Thr1381Ala	missense_variant	28/52	ENST00000261405.10	NP_000543.3	P04275-1
VWF	XM_047429501.1 linkuse as main transcript	c.4141A>G	p.Thr1381Ala	missense_variant	28/52		XP_047285457.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
VWF	ENST00000261405.10 linkuse as main transcript	c.4141A>G	p.Thr1381Ala	missense_variant	28/52	1	NM_000552.5	ENSP00000261405.5		P04275-1
VWF	ENST00000538635.5 linkuse as main transcript	n.421-25343A>G		intron_variant		4

Frequencies

GnomAD3 genomes

AF:

0.715

AC:

108580

AN:

151844

Hom.:

39958

Cov.:

show subpopulations

Gnomad AFR

AF:

0.893

Gnomad AMI

AF:

0.689

Gnomad AMR

AF:

0.753

Gnomad ASJ

AF:

0.684

Gnomad EAS

AF:

0.747

Gnomad SAS

AF:

0.765

Gnomad FIN

AF:

0.549

Gnomad MID

AF:

0.782

Gnomad NFE

AF:

0.619

Gnomad OTH

AF:

0.724

GnomAD3 exomes

AF:

0.686

AC:

170206

AN:

248236

Hom.:

60190

AF XY:

0.681

AC XY:

91505

AN XY:

134344

show subpopulations

Gnomad AFR exome

AF:

0.897

Gnomad AMR exome

AF:

0.806

Gnomad ASJ exome

AF:

0.680

Gnomad EAS exome

AF:

0.762

Gnomad SAS exome

AF:

0.749

Gnomad FIN exome

AF:

0.552

Gnomad NFE exome

AF:

0.616

Gnomad OTH exome

AF:

0.678

GnomAD4 exome

AF:

0.638

AC:

931862

AN:

1461560

Hom.:

301018

Cov.:

AF XY:

0.640

AC XY:

465156

AN XY:

727084

show subpopulations

Gnomad4 AFR exome

AF:

0.905

Gnomad4 AMR exome

AF:

0.802

Gnomad4 ASJ exome

AF:

0.685

Gnomad4 EAS exome

AF:

0.738

Gnomad4 SAS exome

AF:

0.743

Gnomad4 FIN exome

AF:

0.551

Gnomad4 NFE exome

AF:

0.612

Gnomad4 OTH exome

AF:

0.665

GnomAD4 genome

AF:

0.715

AC:

108674

AN:

151962

Hom.:

39998

Cov.:

AF XY:

0.717

AC XY:

53254

AN XY:

74240

show subpopulations

Gnomad4 AFR

AF:

0.893

Gnomad4 AMR

AF:

0.754

Gnomad4 ASJ

AF:

0.684

Gnomad4 EAS

AF:

0.747

Gnomad4 SAS

AF:

0.766

Gnomad4 FIN

AF:

0.549

Gnomad4 NFE

AF:

0.619

Gnomad4 OTH

AF:

0.720

Alfa

AF:

0.658

Hom.:

17198

Bravo

AF:

0.739

TwinsUK

AF:

0.612

AC:

2269

ALSPAC

AF:

0.617

AC:

2377

ESP6500AA

AF:

0.882

AC:

3886

ESP6500EA

AF:

0.620

AC:

5331

ExAC

AF:

0.680

AC:

82506

Asia WGS

AF:

0.772

AC:

2686

AN:

3478

ClinVar

Significance: Benign

Submissions summary: Uncertain:1Benign:11

Revision: reviewed by expert panel

LINK: link

Submissions by phenotype

not provided

Uncertain:1Benign:3

Benign, criteria provided, single submitter	clinical testing	Quest Diagnostics Nichols Institute San Juan Capistrano	Feb 17, 2023	- -
Uncertain significance, no assertion criteria provided	clinical testing	Department of Pathology and Laboratory Medicine, Sinai Health System	-	Allele frequency is common in at least one population database (frequency: 89.735% in gnomAD_Exomes) based on the frequency threshold of 0.5% for this gene. Variant was observed in a homozygous state in population databases more than expected for disease. -
Likely benign, criteria provided, single submitter	not provided	Breakthrough Genomics, Breakthrough Genomics	-	- -
Benign, criteria provided, single submitter	clinical testing	ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories	Apr 13, 2021	- -

not specified

Benign:3

Benign, no assertion criteria provided	clinical testing	Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+	-	- -
Benign, criteria provided, single submitter	clinical testing	PreventionGenetics, part of Exact Sciences	-	- -
Benign, no assertion criteria provided	clinical testing	Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen	-	- -

Hereditary von Willebrand disease

Benign:2

Benign, reviewed by expert panel	curation	ClinGen von Willebrand Disease Variant Curation Expert Panel, ClinGen	Aug 13, 2024	The missense variant NM_000552.5(VWF):c.4141A>G (p.Thr1381Ala) is common in the general population with a Grpmax filtering allele frequency of 0.8925 (based on 67313/74942 alleles in the African/African American population) in gnomAD v4.1 (BA1). Several probands have been reported (PMID: 30817071, PMID: 30762591) with Thr1381Ala in cis or trans with additional vWF variants, including the type 2B Arg1308Cys variant (ClinVar 289, classified Pathogenic by the ClinGen VWD VCEP; BP5). and therefore meets criteria to be classified as benign for von Willebrand disease based on the ACMG/AMP criteria applied, as specified by the ClinGen VWD: BA1, BP4, BP5 (VCEP Rule specifications for von Willebrand disease type 2A, 2B and 2M v1.0.0; 08/12/2024). -
Likely benign, criteria provided, single submitter	clinical testing	Illumina Laboratory Services, Illumina	Jun 14, 2016	- -

von Willebrand disease type 2

Benign:1

Benign, criteria provided, single submitter

clinical testing

Genome-Nilou Lab

Dec 05, 2021

- -

von Willebrand disease type 3

Benign:1

Benign, criteria provided, single submitter

clinical testing

Genome-Nilou Lab

Dec 05, 2021

- -

von Willebrand disease type 1

Benign:1

Benign, criteria provided, single submitter

clinical testing

Genome-Nilou Lab

Dec 05, 2021

- -

Computational scores

Source: dbNSFP v4.3

Name

Calibrated prediction

Score

Prediction

AlphaMissense

Benign

0.070

BayesDel_addAF

Benign

-0.63

BayesDel_noAF

Benign

-0.53

CADD

Benign

0.14

DANN

Benign

0.18

DEOGEN2

Benign

0.33

Eigen

Benign

-1.8

Eigen_PC

Benign

-1.6

FATHMM_MKL

Benign

0.0011

LIST_S2

Benign

0.34

MetaRNN

Benign

0.0000053

MetaSVM

Benign

-0.97

MutationAssessor

Benign

-2.1

PrimateAI

Benign

0.27

PROVEAN

Benign

1.1

REVEL

Benign

0.19

Sift

Benign

1.0

Sift4G

Benign

1.0

Polyphen

0.0

Vest4

0.045

MPC

0.26

ClinPred

0.0086

GERP RS

0.20

Varity_R

0.11

gMVP

0.56

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

Below is the list of publications found by LitVar. It may be empty.

Variant summary

Frequency

Consequence

Scores

Clinical Significance

Conservation

ACMG classification

Transcripts

RefSeq

Ensembl

Frequencies

ClinVar

Submissions by phenotype

Computational scores

Splicing

Publications

LitVar

Other links and lift over