chr3:10142038:G>A Detail (hg38) (VHL)

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

Genome

Assembly	Position
hg19	chr3:10,183,722-10,183,722 View the variant detail on this assembly version.
hg38	chr3:10,142,038-10,142,038

HGVS

VHL

Type	Transcript	Protein
RefSeq	NM_000551.3:c.191G>A	NP_000542.1:p.Arg64His
	NM_198156.2:c.191G>A	NP_937799.1:p.Arg64His
Ensemble	ENST00000256474.3:c.191G>A	ENST00000256474.3:p.Arg64His
	ENST00000345392.3:c.191G>A	ENST00000345392.3:p.Arg64His
	ENST00000696143.2:c.191G>A	ENST00000696143.2:p.Arg64His
	ENST00000696153.1:c.191G>A	ENST00000696153.1:p.Arg64His
	ENST00000713811.1:c.191G>A	ENST00000713811.1:p.Arg64His
	ENST00000713812.1:c.191G>A	ENST00000713812.1:p.Arg64His
	ENST00000713815.1:c.36+155G>A
	ENST00000713982.1:c.191G>A	ENST00000713982.1:p.Arg64His

Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics	Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance	Uncertain significance
Review star
Show details

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
	MONDO

Disease area statistics

[No Data.]

MGeND

[No Data.]

ClinVar

Clinical significance	Last evaluated	Review status	Condition	Origin	Links
Uncertain significance	2023-08-02	criteria provided, single submitter	Von Hippel-Lindau syndrome,Chuvash polycythemia	germline	Detail
Uncertain significance	2023-08-02	criteria provided, single submitter	Von Hippel-Lindau syndrome,Chuvash polycythemia	germline	Detail
Uncertain significance	2019-06-25	criteria provided, single submitter	not provided	germline	Detail

CIViC

[No Data.]

DisGeNET

Score	Disease name	Description	Source	Pubmed	Links
0.125	Neoplastic Syndromes, Hereditary	NA	CLINVAR		Detail
0.416	pheochromocytoma	NA	CLINVAR		Detail

Annotation

Annotations

Descrption	Source	Links
NM_000551.4(VHL):c.191G>A (p.Arg64His) AND multiple conditions	ClinVar	Detail
NM_000551.4(VHL):c.191G>A (p.Arg64His) AND multiple conditions	ClinVar	Detail
NM_000551.4(VHL):c.191G>A (p.Arg64His) AND not provided	ClinVar	Detail
NA	DisGeNET	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: rs104893826 dbSNP
Genome: hg38
Position: chr3:10,142,038-10,142,038
Variant Type: snv
Reference Allele: G
Alternative Allele: A

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