chr1:155206167:C>T Detail (hg19) (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	chr1:155,206,167-155,206,167
hg38	chr1:155,236,376-155,236,376 View the variant detail on this assembly version.

HGVS

GBA1

Type	Transcript	Protein
RefSeq	NM_001005741.2:c.1093G>A	NP_001005741.1:p.Glu365Lys
	NM_001005742.2:c.1093G>A	NP_001005742.1:p.Glu365Lys
	NM_001171811.1:c.832G>A	NP_001165282.1:p.Glu278Lys
	NM_001171812.1:c.946G>A	NP_001165283.1:p.Glu316Lys
	NM_000157.3:c.1093G>A	NP_000148.2:p.Glu365Lys
Ensemble	ENST00000327247.9:c.1093G>A	ENST00000327247.9:p.Glu365Lys
	ENST00000428024.3:c.832G>A	ENST00000428024.3:p.Glu278Lys
	ENST00000427500.7:c.946G>A	ENST00000427500.7:p.Glu316Lys
	ENST00000368373.8:c.1093G>A	ENST00000368373.8:p.Glu365Lys

Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics	Show details

Frequency

JP	HGVD:[No Data.]
	ToMMo:[No Data.]
	NCBN:[No Data.]
	NCBN(Hondo):[No Data.]
	NCBN(Ryukyu):[No Data.]
East asia	ExAC:<0.001

Prediction

ClinVar

Clinical Significance	Benign Likely benign; risk factor
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
	COSMIC
	MONDO

Disease area statistics

[No Data.]

MGeND

[No Data.]

ClinVar

Clinical significance	Last evaluated	Review status	Condition	Origin	Links
Pathogenic	2004-06-01	no assertion criteria provided	Gaucher disease type I	germline	Detail
Benign Likely benign	2020-05-25	criteria provided, multiple submitters, no conflicts	not specified	germline	Detail
risk factor	2014-12-12	criteria provided, single submitter	Parkinsonian disorder	unknown	Detail
risk factor	2014-02-17	criteria provided, single submitter	Parkinsonian disorder	unknown	Detail
risk factor	2014-06-19	criteria provided, single submitter	Parkinsonian disorder,Hypertensive disorder	unknown	Detail
risk factor	2014-06-19	criteria provided, single submitter	Parkinsonian disorder,Hypertensive disorder	unknown	Detail
Benign	2024-04-01	criteria provided, multiple submitters, no conflicts	not provided	germline unknown	Detail
Benign	2020-01-22	criteria provided, single submitter	Gaucher disease	germline	Detail
Likely benign	2021-05-18	criteria provided, single submitter	Gaucher disease perinatal lethal	germline	Detail
risk factor	2021-05-03	criteria provided, single submitter	Parkinson disease, late-onset	germline	Detail

CIViC

[No Data.]

DisGeNET

Score	Disease name	Description	Source	Pubmed	Links
0.445	Gaucher Disease, Type 1	NA	CLINVAR		Detail
0.445	Gaucher Disease, Type 1	Analysis and classification of 304 mutant alleles in patients with type 1 and ty...	UNIPROT	10796875	Detail

Annotation

Annotations

Descrption	Source	Links
NM_001005741.2(GBA1):c.[535G>C;c.1093G>A] AND Gaucher disease type I	ClinVar	Detail
NM_000157.4(GBA1):c.1093G>A (p.Glu365Lys) AND not specified	ClinVar	Detail
NM_000157.4(GBA1):c.1093G>A (p.Glu365Lys) AND multiple conditions	ClinVar	Detail
NM_000157.4(GBA1):c.1093G>A (p.Glu365Lys) AND Parkinsonian disorder	ClinVar	Detail
NM_000157.4(GBA1):c.1093G>A (p.Glu365Lys) AND multiple conditions	ClinVar	Detail
NM_000157.4(GBA1):c.1093G>A (p.Glu365Lys) AND multiple conditions	ClinVar	Detail
NM_000157.4(GBA1):c.1093G>A (p.Glu365Lys) AND not provided	ClinVar	Detail
NM_000157.4(GBA1):c.1093G>A (p.Glu365Lys) AND Gaucher disease	ClinVar	Detail
NM_000157.4(GBA1):c.1093G>A (p.Glu365Lys) AND Gaucher disease perinatal lethal	ClinVar	Detail
NM_000157.4(GBA1):c.1093G>A (p.Glu365Lys) AND Parkinson disease, late-onset	ClinVar	Detail
NA	DisGeNET	Detail
Analysis and classification of 304 mutant alleles in patients with type 1 and type 3 Gaucher disease...	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: rs2230288 dbSNP
Genome: hg19
Position: chr1:155,206,167-155,206,167
Variant Type: snv
Reference Allele: C
Alternative Allele: T
East Asian Chromosome Counts (ExAC): 8650
East Asian Allele Counts (ExAC): 2
East Asian Heterozygous Counts (ExAC): 2
East Asian Homozygous Counts (ExAC): 0
East Asian Allele Frequency (ExAC): 2.3121387283236994E-4
Chromosome Counts in All Race (ExAC): 121320
Allele Counts in All Race (ExAC): 1188
Heterozygous Counts in All Race (ExAC): 1164
Homozygous Counts in All Race (ExAC): 12
Allele Frequency in All Race (ExAC): 0.009792284866468843

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