chr11:6412649:C> Detail (hg19) (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	chr11:6,412,649-6,412,649
hg38	chr11:6,391,419-6,391,419

HGVS

SMPD1

Type	Transcript	Protein
RefSeq	NM_000543.4:c.354delC	NP_000534.3:p.Ile119SerfsTer7
	NM_001007593.2:c.354delC	NP_001007594.2:p.Ile119SerfsTer7
	NM_001318087.1:c.354delC	NP_001305016.1:p.Ile119SerfsTer7
Ensemble	ENST00000527275.5:c.351delC	ENST00000527275.5:p.Ile118SerfsTer7
	ENST00000342245.9:c.354delC	ENST00000342245.9:p.Ile119SerfsTer7

Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics	Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance	Pathogenic Likely pathogenic
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
	COSMIC
	MONDO

Disease area statistics

[No Data.]

MGeND

[No Data.]

ClinVar

Clinical significance	Last evaluated	Review status	Condition	Origin	Links
Pathogenic Likely pathogenic	2022-07-13	criteria provided, multiple submitters, no conflicts	not provided	germline	Detail
Pathogenic Likely pathogenic	2023-06-11	criteria provided, multiple submitters, no conflicts	Niemann-Pick disease, type A	germline unknown	Detail
Pathogenic	2023-06-11	criteria provided, single submitter	Niemann-Pick disease, type B,Niemann-Pick disease, type A	germline	Detail
Pathogenic	2023-06-11	criteria provided, single submitter	Niemann-Pick disease, type B,Niemann-Pick disease, type A	germline	Detail

CIViC

[No Data.]

DisGeNET

Score	Disease name	Description	Source	Pubmed	Links
0.565	Niemann-Pick disease, type B	NA	CLINVAR		Detail

Annotation

Annotations

Descrption	Source	Links
NM_000543.5(SMPD1):c.354del (p.Ile119fs) AND not provided	ClinVar	Detail
NM_000543.5(SMPD1):c.354del (p.Ile119fs) AND Niemann-Pick disease, type A	ClinVar	Detail
NM_000543.5(SMPD1):c.354del (p.Ile119fs) AND multiple conditions	ClinVar	Detail
NM_000543.5(SMPD1):c.354del (p.Ile119fs) 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: rs727504165 dbSNP
Genome: hg19
Position: chr11:6,412,649-6,412,649
Variant Type: snv
Reference Allele: C
Alternative Allele: -

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