chr1:155236277:G>A Detail (hg38) (GBA1, LOC106627981)

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

Genome

Assembly	Position
hg19	chr1:155,206,068-155,206,068 View the variant detail on this assembly version.
hg38	chr1:155,236,277-155,236,277

HGVS

GBA1

Type	Transcript	Protein
RefSeq	NM_001005741.2:c.1192C>T	NP_001005741.1:p.Arg398Ter
	NM_001005742.2:c.1192C>T	NP_001005742.1:p.Arg398Ter
	NM_000157.3:c.1192C>T	NP_000148.2:p.Arg398Ter
	NM_001171812.1:c.1045C>T	NP_001165283.1:p.Arg349Ter
	NM_001171811.1:c.931C>T	NP_001165282.1:p.Arg311Ter
Ensemble	ENST00000327247.9:c.1192C>T	ENST00000327247.9:p.Arg398Ter
	ENST00000368373.8:c.1192C>T	ENST00000368373.8:p.Arg398Ter
	ENST00000427500.7:c.1045C>T	ENST00000427500.7:p.Arg349Ter
	ENST00000428024.3:c.931C>T	ENST00000428024.3:p.Arg311Ter

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

GBA1

Type	Database	ID	Link
Gene	MIM	606463	OMIM
	HGNC	4177	HGNC
	Ensembl	ENSG00000177628	Ensembl
	NCBI		NCBI
	Gene Cards		Gene Cards
	OncoKB		OncoKB

Type	Database	ID	Link
Variant	TogoVar	tgv184505705	TogoVar
	COSMIC	COSM1207959	COSMIC
	MONDO

Disease area statistics

[No Data.]

MGeND

[No Data.]

ClinVar

Clinical significance	Last evaluated	Review status	Condition	Origin	Links
Pathogenic	1999-05-01	no assertion criteria provided	Gaucher disease perinatal lethal	germline	Detail
Pathogenic	2023-12-01	criteria provided, multiple submitters, no conflicts	not provided	germline	Detail
Pathogenic	2018-09-24	criteria provided, single submitter	Gaucher disease	germline	Detail
Pathogenic	2020-01-22	criteria provided, single submitter	Gaucher disease type I	germline	Detail
Pathogenic	2022-04-11	criteria provided, single submitter	Parkinson disease, late-onset,Gaucher disease type III,Gaucher disease type II,Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome,Gaucher disease type I,Gaucher disease perinatal lethal,Lewy body dementia	unknown	Detail
Pathogenic	2022-04-11	criteria provided, single submitter	Parkinson disease, late-onset,Gaucher disease type III,Gaucher disease type II,Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome,Gaucher disease type I,Gaucher disease perinatal lethal,Lewy body dementia	unknown	Detail
Pathogenic	2022-04-11	criteria provided, single submitter	Parkinson disease, late-onset,Gaucher disease type III,Gaucher disease type II,Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome,Gaucher disease type I,Gaucher disease perinatal lethal,Lewy body dementia	unknown	Detail
Pathogenic	2022-04-11	criteria provided, single submitter	Parkinson disease, late-onset,Gaucher disease type III,Gaucher disease type II,Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome,Gaucher disease type I,Gaucher disease perinatal lethal,Lewy body dementia	unknown	Detail
Pathogenic	2022-04-11	criteria provided, single submitter	Parkinson disease, late-onset,Gaucher disease type III,Gaucher disease type II,Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome,Gaucher disease type I,Gaucher disease perinatal lethal,Lewy body dementia	unknown	Detail
Pathogenic	2022-04-11	criteria provided, single submitter	Parkinson disease, late-onset,Gaucher disease type III,Gaucher disease type II,Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome,Gaucher disease type I,Gaucher disease perinatal lethal,Lewy body dementia	unknown	Detail
Pathogenic	2022-04-11	criteria provided, single submitter	Parkinson disease, late-onset,Gaucher disease type III,Gaucher disease type II,Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome,Gaucher disease type I,Gaucher disease perinatal lethal,Lewy body dementia	unknown	Detail

CIViC

[No Data.]

DisGeNET

Score	Disease name	Description	Source	Pubmed	Links
0.445	Gaucher Disease, Type 1	NA	CLINVAR		Detail
0.360	GAUCHER DISEASE, PERINATAL LETHAL	NA	CLINVAR		Detail

Annotation

Annotations

Descrption	Source	Links
NM_000157.4(GBA1):c.1192C>T (p.Arg398Ter) AND Gaucher disease perinatal lethal	ClinVar	Detail
NM_000157.4(GBA1):c.1192C>T (p.Arg398Ter) AND not provided	ClinVar	Detail
NM_000157.4(GBA1):c.1192C>T (p.Arg398Ter) AND Gaucher disease	ClinVar	Detail
NM_000157.4(GBA1):c.1192C>T (p.Arg398Ter) AND Gaucher disease type I	ClinVar	Detail
NM_000157.4(GBA1):c.1192C>T (p.Arg398Ter) AND multiple conditions	ClinVar	Detail
NM_000157.4(GBA1):c.1192C>T (p.Arg398Ter) AND multiple conditions	ClinVar	Detail
NM_000157.4(GBA1):c.1192C>T (p.Arg398Ter) AND multiple conditions	ClinVar	Detail
NM_000157.4(GBA1):c.1192C>T (p.Arg398Ter) AND multiple conditions	ClinVar	Detail
NM_000157.4(GBA1):c.1192C>T (p.Arg398Ter) AND multiple conditions	ClinVar	Detail
NM_000157.4(GBA1):c.1192C>T (p.Arg398Ter) AND multiple conditions	ClinVar	Detail
NM_000157.4(GBA1):c.1192C>T (p.Arg398Ter) AND multiple conditions	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: rs121908309 dbSNP
Genome: hg38
Position: chr1:155,236,277-155,236,277
Variant Type: snv
Reference Allele: G
Alternative Allele: A

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