chr11:6391657:G>C Detail (hg38) (SMPD1)

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

Genome

Assembly	Position
hg19	chr11:6,412,887-6,412,887 View the variant detail on this assembly version.
hg38	chr11:6,391,657-6,391,657

HGVS

SMPD1

Type	Transcript	Protein
RefSeq	NM_000543.4:c.592G>C	NP_000534.3:p.Ala198Pro
	NM_001007593.2:c.592G>C	NP_001007594.2:p.Ala198Pro
	NM_001318087.1:c.592G>C	NP_001305016.1:p.Ala198Pro
Ensemble	ENST00000342245.9:c.592G>C	ENST00000342245.9:p.Ala198Pro
	ENST00000527275.5:c.589G>C	ENST00000527275.5:p.Ala197Pro

Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics	Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance	Conflicting classifications of pathogenicity
Review star
Show details

Links

SMPD1

Type	Database	ID	Link
Gene	MIM	607608	OMIM
	HGNC	11120	HGNC
	Ensembl	ENSG00000166311	Ensembl
	NCBI		NCBI
	Gene Cards		Gene Cards
	OncoKB		OncoKB

Type	Database	ID	Link
Variant	TogoVar	tgv41491823	TogoVar
	COSMIC
	MONDO

Disease area statistics

[No Data.]

MGeND

[No Data.]

ClinVar

Clinical significance	Last evaluated	Review status	Condition	Origin	Links
Uncertain significance	2020-01-22	criteria provided, single submitter	Sphingomyelin/cholesterol lipidosis	germline	Detail
Pathogenic		criteria provided, single submitter	Niemann-Pick disease, type A	germline	Detail
Pathogenic	2019-01-21	criteria provided, single submitter	Niemann-Pick disease, type B	germline	Detail
Pathogenic	2023-11-05	criteria provided, single submitter	Niemann-Pick disease, type A,Niemann-Pick disease, type B	germline	Detail
Pathogenic	2023-11-05	criteria provided, single submitter	Niemann-Pick disease, type A,Niemann-Pick disease, type B	germline	Detail
Likely pathogenic	2023-07-10	criteria provided, single submitter	not provided	germline	Detail

CIViC

[No Data.]

DisGeNET

Score	Disease name	Description	Source	Pubmed	Links
0.266	Niemann-Pick Diseases	NA	CLINVAR		Detail

Annotation

Annotations

Descrption	Source	Links
NM_000543.5(SMPD1):c.592G>C (p.Ala198Pro) AND Sphingomyelin/cholesterol lipidosis	ClinVar	Detail
NM_000543.5(SMPD1):c.592G>C (p.Ala198Pro) AND Niemann-Pick disease, type A	ClinVar	Detail
NM_000543.5(SMPD1):c.592G>C (p.Ala198Pro) AND Niemann-Pick disease, type B	ClinVar	Detail
NM_000543.5(SMPD1):c.592G>C (p.Ala198Pro) AND multiple conditions	ClinVar	Detail
NM_000543.5(SMPD1):c.592G>C (p.Ala198Pro) AND multiple conditions	ClinVar	Detail
NM_000543.5(SMPD1):c.592G>C (p.Ala198Pro) AND not provided	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: rs797044798 dbSNP
Genome: hg38
Position: chr11:6,391,657-6,391,657
Variant Type: snv
Reference Allele: G
Alternative Allele: C

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