chr1:155206217:G>C 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	chr1:155,206,217-155,206,217
hg38	chr1:155,236,426-155,236,426 View the variant detail on this assembly version.

HGVS

GBA1

Type	Transcript	Protein
RefSeq	NM_001005741.2:c.1043C>G	NP_001005741.1:p.Ala348Gly
	NM_001005742.2:c.1043C>G	NP_001005742.1:p.Ala348Gly
	NM_001171811.1:c.782C>G	NP_001165282.1:p.Ala261Gly
	NM_000157.3:c.1043C>G	NP_000148.2:p.Ala348Gly
	NM_001171812.1:c.896C>G	NP_001165283.1:p.Ala299Gly
Ensemble	ENST00000327247.9:c.1043C>G	ENST00000327247.9:p.Ala348Gly
	ENST00000428024.3:c.782C>G	ENST00000428024.3:p.Ala261Gly
	ENST00000368373.8:c.1043C>G	ENST00000368373.8:p.Ala348Gly
	ENST00000427500.7:c.896C>G	ENST00000427500.7:p.Ala299Gly

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	Uncertain significance
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
Uncertain significance	2019-08-26	criteria provided, single submitter	not provided	germline	Detail
Uncertain significance	2022-03-15	criteria provided, single submitter	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome,Gaucher disease type II,Lewy body dementia,Gaucher disease type I,Gaucher disease type III,Parkinson disease, late-onset,Gaucher disease perinatal lethal	unknown	Detail
Uncertain significance	2022-03-15	criteria provided, single submitter	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome,Gaucher disease type II,Lewy body dementia,Gaucher disease type I,Gaucher disease type III,Parkinson disease, late-onset,Gaucher disease perinatal lethal	unknown	Detail
Uncertain significance	2022-03-15	criteria provided, single submitter	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome,Gaucher disease type II,Lewy body dementia,Gaucher disease type I,Gaucher disease type III,Parkinson disease, late-onset,Gaucher disease perinatal lethal	unknown	Detail
Uncertain significance	2022-03-15	criteria provided, single submitter	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome,Gaucher disease type II,Lewy body dementia,Gaucher disease type I,Gaucher disease type III,Parkinson disease, late-onset,Gaucher disease perinatal lethal	unknown	Detail
Uncertain significance	2022-03-15	criteria provided, single submitter	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome,Gaucher disease type II,Lewy body dementia,Gaucher disease type I,Gaucher disease type III,Parkinson disease, late-onset,Gaucher disease perinatal lethal	unknown	Detail
Uncertain significance	2022-03-15	criteria provided, single submitter	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome,Gaucher disease type II,Lewy body dementia,Gaucher disease type I,Gaucher disease type III,Parkinson disease, late-onset,Gaucher disease perinatal lethal	unknown	Detail
Uncertain significance	2022-03-15	criteria provided, single submitter	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome,Gaucher disease type II,Lewy body dementia,Gaucher disease type I,Gaucher disease type III,Parkinson disease, late-onset,Gaucher disease perinatal lethal	unknown	Detail

CIViC

[No Data.]

DisGeNET

Score	Disease name	Description	Source	Pubmed	Links
0.445	Gaucher Disease, Type 1	NA	CLINVAR		Detail

Annotation

Annotations

Descrption	Source	Links
NM_000157.4(GBA1):c.1043C>G (p.Ala348Gly) AND not provided	ClinVar	Detail
NM_000157.4(GBA1):c.1043C>G (p.Ala348Gly) AND multiple conditions	ClinVar	Detail
NM_000157.4(GBA1):c.1043C>G (p.Ala348Gly) AND multiple conditions	ClinVar	Detail
NM_000157.4(GBA1):c.1043C>G (p.Ala348Gly) AND multiple conditions	ClinVar	Detail
NM_000157.4(GBA1):c.1043C>G (p.Ala348Gly) AND multiple conditions	ClinVar	Detail
NM_000157.4(GBA1):c.1043C>G (p.Ala348Gly) AND multiple conditions	ClinVar	Detail
NM_000157.4(GBA1):c.1043C>G (p.Ala348Gly) AND multiple conditions	ClinVar	Detail
NM_000157.4(GBA1):c.1043C>G (p.Ala348Gly) AND multiple conditions	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: rs78396650 dbSNP
Genome: hg19
Position: chr1:155,206,217-155,206,217
Variant Type: snv
Reference Allele: G
Alternative Allele: C
East Asian Chromosome Counts (ExAC): 8652
East Asian Allele Counts (ExAC): 0
East Asian Heterozygous Counts (ExAC): 0
East Asian Homozygous Counts (ExAC): 0
East Asian Allele Frequency (ExAC): 0.0
Chromosome Counts in All Race (ExAC): 121170
Allele Counts in All Race (ExAC): 5
Heterozygous Counts in All Race (ExAC): 5
Homozygous Counts in All Race (ExAC): 0
Allele Frequency in All Race (ExAC): 4.126433935792688E-5

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