chr1:155237458:A>C Detail (hg38) (GBA1, LOC106627981)

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

Information

Genome

Assembly	Position
hg19	chr1:155,207,249-155,207,249 View the variant detail on this assembly version.
hg38	chr1:155,237,458-155,237,458

HGVS

GBA1

Type	Transcript	Protein
RefSeq	NM_001005741.2:c.882T>G	NP_001005741.1:p.His294Gln
	NM_001005742.2:c.882T>G	NP_001005742.1:p.His294Gln
	NM_000157.3:c.882T>G	NP_000148.2:p.His294Gln
	NM_001171812.1:c.735T>G	NP_001165283.1:p.His245Gln
	NM_001171811.1:c.621T>G	NP_001165282.1:p.His207Gln
Ensemble	ENST00000327247.9:c.882T>G	ENST00000327247.9:p.His294Gln
	ENST00000368373.8:c.882T>G	ENST00000368373.8:p.His294Gln
	ENST00000427500.7:c.735T>G	ENST00000427500.7:p.His245Gln
	ENST00000428024.3:c.621T>G	ENST00000428024.3:p.His207Gln

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	Conflicting classifications of pathogenicity; other
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	2005-04-01	no assertion criteria provided	Gaucher disease type II	germline	Detail
Pathogenic	2005-04-01	no assertion criteria provided	Gaucher disease type III	germline	Detail
Conflicting interpretations of pathogenicity; other	2024-03-25	criteria provided, conflicting interpretations	not provided	germline unknown	Detail
Likely pathogenic		criteria provided, single submitter	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome,Gaucher disease type I,Gaucher disease type II,Gaucher disease type III	germline	Detail
Likely pathogenic		criteria provided, single submitter	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome,Gaucher disease type I,Gaucher disease type II,Gaucher disease type III	germline	Detail
Likely pathogenic		criteria provided, single submitter	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome,Gaucher disease type I,Gaucher disease type II,Gaucher disease type III	germline	Detail
Likely pathogenic		criteria provided, single submitter	Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome,Gaucher disease type I,Gaucher disease type II,Gaucher disease type III	germline	Detail
Pathogenic	2016-01-01	criteria provided, single submitter	Gaucher disease perinatal lethal	unknown	Detail
Uncertain significance	2020-01-14	criteria provided, single submitter	Gaucher disease	germline	Detail
Conflicting interpretations of pathogenicity	2022-09-28	criteria provided, conflicting interpretations	Gaucher disease type I	germline unknown	Detail
Uncertain significance	2024-03-21	criteria provided, multiple submitters, no conflicts	not specified	germline	Detail

CIViC

[No Data.]

DisGeNET

Score	Disease name	Description	Source	Pubmed	Links
0.441	Gaucher Disease, Type 2 (disorder)	NA	CLINVAR		Detail
0.441	Gaucher Disease, Type 3 (disorder)	NA	CLINVAR		Detail

Annotation

Annotations

Descrption	Source	Links
NM_001005741.2(GBA1):c.[880T>G;1342G>C] AND Gaucher disease type II	ClinVar	Detail
NM_001005741.2(GBA1):c.[880T>G;1342G>C] AND Gaucher disease type III	ClinVar	Detail
NM_000157.4(GBA1):c.882T>G (p.His294Gln) AND not provided	ClinVar	Detail
NM_000157.4(GBA1):c.882T>G (p.His294Gln) AND multiple conditions	ClinVar	Detail
NM_000157.4(GBA1):c.882T>G (p.His294Gln) AND multiple conditions	ClinVar	Detail
NM_000157.4(GBA1):c.882T>G (p.His294Gln) AND multiple conditions	ClinVar	Detail
NM_000157.4(GBA1):c.882T>G (p.His294Gln) AND multiple conditions	ClinVar	Detail
NM_000157.4(GBA1):c.882T>G (p.His294Gln) AND Gaucher disease perinatal lethal	ClinVar	Detail
NM_000157.4(GBA1):c.882T>G (p.His294Gln) AND Gaucher disease	ClinVar	Detail
NM_000157.4(GBA1):c.882T>G (p.His294Gln) AND Gaucher disease type I	ClinVar	Detail
NM_000157.4(GBA1):c.882T>G (p.His294Gln) AND not specified	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: rs367968666 dbSNP
Genome: hg38
Position: chr1:155,237,458-155,237,458
Variant Type: snv
Reference Allele: A
Alternative Allele: C
East Asian Chromosome Counts (ExAC): 8654
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): 121348
Allele Counts in All Race (ExAC): 34
Heterozygous Counts in All Race (ExAC): 34
Homozygous Counts in All Race (ExAC): 0
Allele Frequency in All Race (ExAC): 2.8018591159310413E-4

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