chr11:6413175:C>A Detail (hg19) (SMPD1)

Information

Genome

Assembly Position
hg19 chr11:6,413,175-6,413,175
hg38 chr11:6,391,945-6,391,945 View the variant detail on this assembly version.

HGVS

Type Transcript Protein
RefSeq NM_000543.4:c.880C>A NP_000534.3:p.Gln294Lys
NM_001007593.2:c.880C>A NP_001007594.2:p.Gln294Lys
NM_001318087.1:c.880C>A NP_001305016.1:p.Gln294Lys
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 Pathogenic
Review star
Show details
Links
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 2005-01-01 no assertion criteria provided Niemann-Pick disease, type B germline Detail
Pathogenic 2005-01-01 no assertion criteria provided Niemann-pick disease, intermediate, protracted neurovisceral germline Detail
Pathogenic 2023-10-08 criteria provided, multiple submitters, no conflicts Niemann-Pick disease, type A germline unknown Detail
Pathogenic 2017-11-22 criteria provided, single submitter not specified germline Detail
Pathogenic 2024-01-29 criteria provided, single submitter Niemann-Pick disease, type B,Niemann-Pick disease, type A germline Detail
Pathogenic 2024-01-29 criteria provided, single submitter Niemann-Pick disease, type B,Niemann-Pick disease, type A germline Detail
Pathogenic 2020-01-22 criteria provided, single submitter Sphingomyelin/cholesterol lipidosis germline Detail
Pathogenic 2021-08-20 criteria provided, single submitter Inborn genetic diseases germline Detail
Pathogenic 2023-09-01 criteria provided, single submitter not provided germline Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.565 Niemann-Pick disease, type B NA CLINVAR Detail
0.562 Niemann-Pick disease, type A NA CLINVAR Detail
0.120 NIEMANN-PICK DISEASE, INTERMEDIATE, PROTRACTED NEUROVISCERAL (disorder) NA CLINVAR Detail
Annotation

Annotations

DescrptionSourceLinks
NM_000543.5(SMPD1):c.880C>A (p.Gln294Lys) AND Niemann-Pick disease, type B ClinVar Detail
NM_000543.5(SMPD1):c.880C>A (p.Gln294Lys) AND Niemann-pick disease, intermediate, protracted neurovi... ClinVar Detail
NM_000543.5(SMPD1):c.880C>A (p.Gln294Lys) AND Niemann-Pick disease, type A ClinVar Detail
NM_000543.5(SMPD1):c.880C>A (p.Gln294Lys) AND not specified ClinVar Detail
NM_000543.5(SMPD1):c.880C>A (p.Gln294Lys) AND multiple conditions ClinVar Detail
NM_000543.5(SMPD1):c.880C>A (p.Gln294Lys) AND multiple conditions ClinVar Detail
NM_000543.5(SMPD1):c.880C>A (p.Gln294Lys) AND Sphingomyelin/cholesterol lipidosis ClinVar Detail
NM_000543.5(SMPD1):c.880C>A (p.Gln294Lys) AND Inborn genetic diseases ClinVar Detail
NM_000543.5(SMPD1):c.880C>A (p.Gln294Lys) AND not provided ClinVar Detail
NA DisGeNET 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
rs120074128 dbSNP
Genome
hg19
Position
chr11:6,413,175-6,413,175
Variant Type
snv
Reference Allele
C
Alternative Allele
A
East Asian Chromosome Counts (ExAC)
8648
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)
121346
Allele Counts in All Race (ExAC)
2
Heterozygous Counts in All Race (ExAC)
2
Homozygous Counts in All Race (ExAC)
0
Allele Frequency in All Race (ExAC)
1.6481795856476523E-5
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