chr12:52308229:G>A Detail (hg19) (ACVRL1)

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

Genome

Assembly	Position
hg19	chr12:52,308,229-52,308,229
hg38	chr12:51,914,445-51,914,445 View the variant detail on this assembly version.

HGVS

ACVRL1

Type	Transcript	Protein
RefSeq	NM_000020.2:c.632G>A	NP_000011.2:p.Gly211Asp
	NM_001077401.1:c.674G>A	NP_001070869.1:p.Gly225Asp
Ensemble	ENST00000713619.1:c.632G>A	ENST00000713619.1:p.Gly211Asp
	ENST00000552678.2:c.632G>A	ENST00000552678.2:p.Gly211Asp
	ENST00000547400.6:c.362G>A	ENST00000547400.6:p.Gly121Asp
	ENST00000551576.6:c.632G>A	ENST00000551576.6:p.Gly211Asp
	ENST00000419526.6:c.110G>A	ENST00000419526.6:p.Gly37Asp
	ENST00000388922.9:c.632G>A	ENST00000388922.9:p.Gly211Asp
	ENST00000550683.5:c.674G>A	ENST00000550683.5:p.Gly225Asp

Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics	Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance	Pathogenic Likely pathogenic
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Links

ACVRL1

Type	Database	ID	Link
Gene	MIM	601284	OMIM
	HGNC	175	HGNC
	Ensembl	ENSG00000139567	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
Pathogenic	2003-12-01	no assertion criteria provided	Pulmonary arterial hypertension related to hereditary hemorrhagic telangiectasia	germline	Detail
Pathogenic Likely pathogenic	2019-04-12	criteria provided, multiple submitters, no conflicts	Telangiectasia, hereditary hemorrhagic, type 2	germline unknown	Detail

CIViC

[No Data.]

DisGeNET

Score	Disease name	Description	Source	Pubmed	Links
0.120	HEREDITARY HEMORRHAGIC TELANGIECTASIA-RELATED PULMONARY ARTERIAL HYPERTENSION	NA	CLINVAR		Detail
0.440	OSLER-RENDU-WEBER SYNDROME 2	Molecular and functional analysis identifies ALK-1 as the predominant cause of p...	UNIPROT	14684682	Detail

Annotation

Annotations

Descrption	Source	Links
NM_000020.3(ACVRL1):c.632G>A (p.Gly211Asp) AND Pulmonary arterial hypertension related to hereditary...	ClinVar	Detail
NM_000020.3(ACVRL1):c.632G>A (p.Gly211Asp) AND Telangiectasia, hereditary hemorrhagic, type 2	ClinVar	Detail
NA	DisGeNET	Detail
Molecular and functional analysis identifies ALK-1 as the predominant cause of pulmonary hypertensio...	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: rs28936687 dbSNP
Genome: hg19
Position: chr12:52,308,229-52,308,229
Variant Type: snv
Reference Allele: G
Alternative Allele: A

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