chr3:10188208:G>T Detail (hg19) (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	chr3:10,188,208-10,188,208
hg38	chr3:10,146,524-10,146,524 View the variant detail on this assembly version.

HGVS

VHL

Type	Transcript	Protein
RefSeq	NM_000551.3:c.351G>T	NP_000542.1:p.Trp117Cys
	NM_198156.2:c.341-3263G>T
Ensemble	ENST00000256474.3:c.351G>T	ENST00000256474.3:p.Trp117Cys
	ENST00000345392.3:c.341-3263G>T
	ENST00000696143.2:c.*18-3263G>T
	ENST00000696153.1:c.351G>T	ENST00000696153.1:p.Trp117Cys
	ENST00000713811.1:c.351G>T	ENST00000713811.1:p.Trp117Cys
	ENST00000713812.1:c.230G>T	ENST00000713812.1:p.Gly77Val
	ENST00000713815.1:c.47G>T	ENST00000713815.1:p.Gly16Val
	ENST00000713982.1:c.341-85G>T

Summary

MGeND

Clinical significance	Likely pathogenic
Variant entry	1
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	COSM14328	COSMIC
	MONDO

Disease area statistics

MGeND

Clinical significance	Last evaluated	Condition	Origin	Submission ID	Submitter	Institute	Citation	Comment	Image
Likely pathogenic		other	germline	MGS000001 (TMGS000138)	Kenjiro Kosaki	Keio University

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	2014-04-24	criteria provided, single submitter	not provided	germline	Detail
Pathogenic	2022-03-30	criteria provided, single submitter	Hereditary cancer-predisposing syndrome	germline	Detail

CIViC

Disease	Drug	EL	ET	ED	CS	VO	TR	Pubmed	Links
von Hippel-Lindau disease		C	Predisposing	Supports	Uncertain Significance	Rare Germline	4	7728151	Detail
von Hippel-Lindau disease		C	Predisposing	Supports	Uncertain Significance	Rare Germline	3	9829911	Detail
von Hippel-Lindau disease		C	Predisposing	Supports	Uncertain Significance	Rare Germline	3	9829912	Detail

DisGeNET

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

Annotation

Annotations

Descrption	Source	Links
In a study of 114 unrelated VHL families, 85 germline mutations were found. VHL mutations were detec...	CIViC Evidence	Detail
Germline mutations were found in all 93 families that fulfilled clinical criteria of VHL disease. Mu...	CIViC Evidence	Detail
Screening of 92 unrelated patients with VHL disease revealed 61 DNA variants. No variants were found...	CIViC Evidence	Detail
NM_000551.4(VHL):c.351G>T (p.Trp117Cys) AND Von Hippel-Lindau syndrome	ClinVar	Detail
NM_000551.4(VHL):c.351G>T (p.Trp117Cys) AND not provided	ClinVar	Detail
NM_000551.4(VHL):c.351G>T (p.Trp117Cys) AND Hereditary cancer-predisposing syndrome	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: rs727504215 dbSNP
Genome: hg19
Position: chr3:10,188,208-10,188,208
Variant Type: snv
Reference Allele: G
Alternative Allele: T
Variant (CIViC) (CIViC Variant): W117C (c.351G>T)
Transcript 1 (CIViC Variant): ENST00000256474.2
Variant URL (CIViC Variant): https://civic.genome.wustl.edu/links/variants/1767

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