chr3:10149790:A>G Detail (hg38) (VHL, LOC107303340)

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Summary
Information
Links
Disease area statistics
MGeND
ClinVar
CIViC
DisGeNET
Annotation
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Information

Genome

Assembly	Position
hg19	chr3:10,191,474-10,191,474 View the variant detail on this assembly version.
hg38	chr3:10,149,790-10,149,790

HGVS

VHL

Type	Transcript	Protein
RefSeq	NM_000551.3:c.467A>G	NP_000542.1:p.Tyr156Cys
	NM_198156.2:c.344A>G	NP_937799.1:p.Tyr115Cys
Ensemble	ENST00000256474.3:c.467A>G	ENST00000256474.3:p.Tyr156Cys
	ENST00000345392.3:c.344A>G	ENST00000345392.3:p.Tyr115Cys
	ENST00000696143.2:c.*21A>G
	ENST00000696153.1:c.578A>G	ENST00000696153.1:p.Tyr193Cys
	ENST00000713811.1:c.582A>G	ENST00000713811.1:p.Val194=
	ENST00000713812.1:c.346A>G	ENST00000713812.1:p.Ile116Val
	ENST00000713815.1:c.163A>G	ENST00000713815.1:p.Ile55Val
	ENST00000713982.1:c.372A>G	ENST00000713982.1:p.Val124=

Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics	Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance	Pathogenic
Review star
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Links

VHL

Type	Database	ID	Link
Gene	MIM	608537	OMIM
	HGNC	12687	HGNC
	Ensembl	ENSG00000134086	Ensembl
	NCBI		NCBI
	Gene Cards		Gene Cards
	OncoKB		OncoKB

Type	Database	ID	Link
Variant	TogoVar
	COSMIC	COSM6977325	COSMIC
	MONDO

Disease area statistics

[No Data.]

MGeND

[No Data.]

ClinVar

Clinical significance	Last evaluated	Review status	Condition	Origin	Links
Pathogenic	2016-02-03	criteria provided, single submitter	Von Hippel-Lindau syndrome	germline	Detail
Pathogenic	2017-06-28	criteria provided, single submitter	not provided	germline	Detail
Pathogenic	2022-06-08	criteria provided, single submitter	Hereditary cancer-predisposing syndrome	germline	Detail
Pathogenic	2022-09-01	criteria provided, single submitter	Von Hippel-Lindau syndrome,Chuvash polycythemia	germline	Detail
Pathogenic	2022-09-01	criteria provided, single submitter	Von Hippel-Lindau syndrome,Chuvash polycythemia	germline	Detail

CIViC

Disease	Drug	EL	ET	ED	CS	VO	TR	Pubmed	Links
von Hippel-Lindau disease		C	Predisposing	Supports	Uncertain Significance	Rare Germline	3	9829912	Detail
adrenal gland pheochromocytoma		C	Predisposing	Supports	Uncertain Significance	Rare Germline	3	12000816	Detail
von Hippel-Lindau disease		C	Predisposing	Supports	Uncertain Significance	Rare Germline	2	20660572	Detail
von Hippel-Lindau disease		C	Predisposing	Supports	Uncertain Significance	Rare Germline	3	24132471	Detail

DisGeNET

Score	Disease name	Description	Source	Pubmed	Links
0.658	Von Hippel-Lindau syndrome	NA	CLINVAR		Detail

Annotation

Annotations

Descrption	Source	Links
Screening of 92 unrelated patients with VHL disease revealed 61 DNA variants. No variants were found...	CIViC Evidence	Detail
Peripheral blood from unrelated patients with pheochromocytoma was tested for mutations of proto-onc...	CIViC Evidence	Detail
53 patients with a molecularly confirmed VHL mutation and a pancreatic neuroendocrine tumor were col...	CIViC Evidence	Detail
Data was collected from 82 VHL mutation carriers in the Dutch VHL surveillance program. Seven patien...	CIViC Evidence	Detail
NM_000551.4(VHL):c.467A>G (p.Tyr156Cys) AND Von Hippel-Lindau syndrome	ClinVar	Detail
NM_000551.4(VHL):c.467A>G (p.Tyr156Cys) AND not provided	ClinVar	Detail
NM_000551.4(VHL):c.467A>G (p.Tyr156Cys) AND Hereditary cancer-predisposing syndrome	ClinVar	Detail
NM_000551.4(VHL):c.467A>G (p.Tyr156Cys) AND multiple conditions	ClinVar	Detail
NM_000551.4(VHL):c.467A>G (p.Tyr156Cys) AND multiple conditions	ClinVar	Detail
NA	DisGeNET	Detail

Overlapped Transcript Coordinates

Gene	Transcript ID	Exon Number	Chromosome	Start	Stop	Type	Amino Mutation	Transcript Position	Links

Overlapped Transcript

Gene	Transcript ID	Chromosome	Start	Stop	Links

Gene: -
dbSNP: rs397516441 dbSNP
Genome: hg38
Position: chr3:10,149,790-10,149,790
Variant Type: snv
Reference Allele: A
Alternative Allele: G
Variant (CIViC) (CIViC Variant): Y156C (c.467A>G)
Transcript 1 (CIViC Variant): ENST00000256474.2
Variant URL (CIViC Variant): https://civic.genome.wustl.edu/links/variants/1946

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